Synthesis and antiradical/antioxidant activities of caffeic acid phenethyl ester and its related propionic, acetic, and benzoic acid analogues

Article abstract of DOI:10.3390/molecules171214637

Caffeic acid phenethyl ester (CAPE) is a bioactive component isolated from propolis. A series of CAPE analogues was synthesized and their antiradical/antioxidant effects analyzed. The effect of the presence of the double bond and of the conjugated system on the antioxidant effect is evaluated with the analogues obtained from 3-(3,4-dihydroxyphenyl) propanoic acid. Those obtained from 2-(3,4-dihydroxyphenyl) acetic acid and 3,4-dihydroxybenzoic acid allow the evaluation of the effect of the presence of two carbons between the carbonyl and aromatic system.

Full text of DOI:10.3390/molecules171214637

Molecules 2012, 17, 14637-14650; doi:10.3390/molecules171214637
OPEN ACCESS
molecules
ISSN 1420-3049
www.mdpi.com/journal/molecules
Article
Synthesis and Antiradical/Antioxidant Activities of Caffeic Acid
Phenethyl Ester and Its Related Propionic, Acetic, and
Benzoic Acid Analogues
Luc M. LeBlanc, Aurélie F. Paré, Jacques Jean-François, Martin J. G. Hébert, Marc E. Surette
and Mohamed Touaibia *
Department of Chemistry and Biochemistry, Université de Moncton, Moncton, NB E1A 3E9, Canada;
E-Mails: LC280974@dal.ca (L.M.L.); aurelie.pare@usherbrooke.ca (A.F.P.);
jacques.jean-francois@umoncton.ca (J.J.-F.); emh3363@umoncton.ca (M.J.G.H.);
marc.surette@umoncton.ca (M.E.S.)
* Author to whom correspondence should be addressed; E-Mail: mohamed.touaibia@umoncton.ca;
Tel.: +1-506-858-4493; Fax: +1-506-858-4541.
Received: 25 October 2012; in revised form: 9 November 2012 / Accepted: 5 December 2012 /
Published: 10 December 2012
Abstract: Caffeic acid phenethyl ester (CAPE) is a bioactive component isolated from
propolis. A series of CAPE analogues was synthesized and their antiradical/antioxidant
effects analyzed. The effect of the presence of the double bond and of the conjugated
system on the antioxidant effect is evaluated with the analogues obtained from
3-(3,4-dihydroxyphenyl) propanoic acid. Those obtained from 2-(3,4-dihydroxyphenyl)
acetic acid and 3,4-dihydroxybenzoic acid allow the evaluation of the effect of the presence
of two carbons between the carbonyl and aromatic system.
Keywords: CAPE; caffeic acid; 3-(3,4-dihydroxyphenyl) propanoic acid esters;
2-(3,4-dihydroxyphenyl) acetic acid esters; 3,4-dihydroxybenzoic acid esters; antioxidant
1. Introduction
From ancient times to nowadays, whether on an empirical or rational basis, natural-based molecules
have long been used as drugs or drug leads. Several small molecules available worldwide on the drug
market can be traced back to or were inspired by natural products [1]. In the ongoing search for new
therapeutic compounds, phenolic acids, which are widely distributed in plants [2], are very important

Molecules 2012, 17
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because of their interactions with several biological targets. Many phenolic acids are linked to cell wall
components such as arabinoxylans and proteins [3,4] and are used as antioxidants in various food
ingredients, such as fatty acids and oils [5,6]. Other uses of phenolic acids include the fortification of
diets in order to provide antimutagenic, antiglycemic, and antioxidative benefits. Such general
characteristics of phenolic acids can be exploited to develop health foods [7].
Caffeic acid, the main representative of the hydroxycinnamic and phenolic acids, is found in many
plants as simple derivatives such as glycosides, amides, esters and sugar esters. Caffeic acid
phenylethyl ester (CAPE), one of the most active compounds in propolis, is the perfect illustration of a
natural compound exhibiting diverse biological activities. Numerous studies have shown that CAPE
has antioxidant, anti-inflammatory, antitumoral, and antifungal activities [8–10]. CAPE’s strong
antioxidant effect can result from transcriptional inhibition of NF-κB and a diminished expression of
pro-inflammatory genes [9,11]. Free radical scavenging, metal ion chelation and inhibition of specific
enzymes that induce free radical or lipid peroxidation are acknowledged as the diverse mechanisms
used by CAPE in its antioxidant activity [12,13]. Based on these promising results, several groups
have started to explore strategies for the synthesis of caffeic acid or CAPE analogues with improved
biological activities.
The antioxidant activities of caffeic acid and CAPE analogues are based on structural factors as
well as the medium used to assay these activities. Son and Lewis, using an aqueous dispersion of
linoleic acid (lipid peroxidation assay), showed that free radical scavenging activity was dependent on
the presence and the number of catechol and hydroxyl groups present, and also on the number of H
donating groups. In the emulsion medium used for the assay, the hydrophobicity of the analogues was
also an important factor in determining their activity [14]. In addition to these known structural
features, it was further demonstrated that phenolic acids bearing a carbonyl group separated from the
aromatic ring were more active (cinnamic acid, caffeic acid) than their counterparts where the carbonyl
is directly linked to the aromatic ring (benzoic acid) [15].
Jayaprakasam and co-workers synthesized a series of caffeic acid analogues with variable alkyl
chain lengths. The antioxidant activity of these compounds was measured by the lipid peroxidation
assay. In the lipophilic medium used for this test, the more lipophilic, long-chain alkyl esters (C16–C22)
were the most potent antioxidants. Compounds with medium alkyl chain length (C4–C8) were less
active (<20% inhibition) compared to caffeic acid (>80% inhibition) [16]. To further assess the
structural parameters related to antioxidant activity, Silva and co-workers synthesized three alkyl
(methyl, ethyl, and propyl) derivatives of caffeic and dihydrocaffeic acids. The radical scavenging
activity of both classes of molecules was evaluated with the 2,2-diphenyl-1-picrylhydrazyl (DPPH)
assay. With the exception of caffeic acid, most of the tested compounds, including dihydroxycaffeic
acid, showed better radical scavenging than α-tocopherol, a reference compound. The ethylene moiety
didn’t influence radical scavenging activity since dihydrocaffeic acid was more potent than caffeic
acid. Increasing the alkyl chain length in a modest fashion, from methyl to propyl, has no significant
effect on radical scavenging activity [17].
Using a Knoevenagel condensation, Zhang and co-workers synthesized a caffeic acid derivative,
namely caffeic acid 3,4-dihydroxyphenethy ester, in high yield. Radical scavenging activity was
evaluated with the DPPH assay and it appears that the 3,4-dihydroxyphenethyl ester analogue shows
strong radical scavenging activity [18]. Caffeic acid is prone to oxidative dimerization [19].

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In natural compounds such as caffeoylquininic acid, where two or three caffeoyl moieties might be
present, such dimerization could influence the antioxidant activity of the molecules. To address this
issue, Saito and co-workers synthesized 6 regio- and stereoisomers of dicaffeoyloxycyclohexanes and
2,4-di-O-caffeoyl-1, 6-anhydro-β-D-glucose as model compounds to evaluate the effect of intramolecular
coupling between two adjacent caffeoyl residues. The radical scavenging activity of these compounds
was evaluated with the DPPH and ABTS (2,2'-azino-bis(3-ethylbenzothiazoline-6-sulphonic acid)
assays and compared against cyclohexyl caffeate. The results underlined the importance of the
orientation or the distance between two adjacent caffeoyl moieties on antioxidant activity. Thus, the
radical scavenging activity was at its lowest with compounds where the two caffeoyl residues were too
far apart to interact. The highest activity was shown by the compound where the diaxial conformations of
the two caffeoyl residues maximize their interaction [20].
Owing to the biological significance of caffeic acid analogues, we report herein the synthesis
of phenethyl and phenpropyl esters of caffeic acid, 3-(3,4-dihydroxyphenyl) propanoic acid
2-(3,4-dihydroxyphenyl) acetic acid, and 3,4-dihydroxybenzoic acid. The antioxidant activity of the
synthesized derivatives was investigated using two tests. Antioxidants employ two major strategies to
deactivate radicals: hydrogen atom transfer (HAT) and electron transfer (ET) [21]. To evaluate which
mechanism was favored by our test compounds we used two different tests. The DPPH assay was used
to evaluate the free radical scavenging activity of the test molecules by an ET reaction. The APPH
(2,2'-azobis(2-amidinopropane) dihydrochloride) assay was used to determine the antioxidant activity
via an HAT mechanism mainly by assessing the prevention of lipid peroxidation in an emulsion
system [22]. The present structure-activity relationship (SAR) study examines the effect of
hydrogenation and the shrinking of the linker between the catechol moiety and the carbonyl on
antioxidant activity. The lengthening of the linker from phenethyl to phenpropyl is also investigated.
2. Results and Discussion
2.1. Synthesis
The syntheses of the phenethyl and phenpropyl esters of caffeic acid as well as the corresponding
3-(3,4-dihydroxyphenyl) propanoic esters are depicted in Scheme 1. Commercially available caffeic
acid (1) is treated with sodium hydroxide and acetic anhydride at 0 °C. Recrystallization of the crude
product from ethanol provides pure diacetylcaffeic acid (2) [23] in good yield. Esters 3 [24] and 4 were
synthesized from 2-phenylethanol or 3-phenylpropanol and acetylated caffeic acid 2. The conversion
of 2 into the corresponding carboxylic chloride was achieved by the Vilsmeier-Haack adduct [25]
derived from thionyl chloride with N,N-dimethylformamide (DMF) as catalyst. As shown in Scheme 1,
phenethyl (CAPE) and phenpropyl esters of caffeic acid 5 [24] and 6, were efficiently obtained by
base-induced de-O-acetylation. Subsequently, esters 5 and 6 were converted into corresponding
3-(3,4-dihydroxyphenyl) propanoic esters 7 and 8 by hydrogenation over a palladium catalyst.
3-(3,4-Dihydroxyphenyl) propanoic acid (dihydrocaffeic acid, 9), was also obtained by hydrogenation
of caffeic acid under the same conditions.

Molecules 2012, 17
Scheme 1. Synthesis of caffeic acid and 3-(3,4-dihydroxyphenyl) propanoic acid esters.
14640
O
O
O
RO
RO
RO
RO
RO
RO
ii
iv
( )
( )
O
OH
O
n
n
3-4; n = 1, 2; R = Ac
5 (CAPE)-6; n = 1, 2; R = H
7-8; n = 1, 2; R = H
1; R = H
iii
i
2; R = Ac
Reagents and conditions: (i) Ac2O, NaOH, 0 °C; (ii) SOCl2, DMF, HO(CH2)2Ph or HO(CH2)3Ph,
Et3N, CH2Cl2, rt; (iii) guanidine·HCl, Et3N, CH2Cl2, MeOH; (iv) H2, Pd/C (10%), MeOH, rt.
As shown in Scheme 2, 2-(3,4-dihydroxyphenyl) acetic phenethyl and phenpropyl esters 14, 15 in
which one carbon separates the carbonyl group from the catechol moiety were also synthesized.
Synthesis began with the protection of the two hydroxyl groups of the commercially available
2-(3,4-dihydroxyphenyl) acetic acid (3,4-DOPAC, 10) by acetate groups in acetic anhydride in the
presence of sulfuric acid. As with 3 and 4, 2-(3,4-dihydroxyphenyl) acetic esters 14 and 15 were
obtained after the conversion of 11 into the corresponding carboxylic chloride, reaction with
2-phenylethanol or 3-phenylpropanol in presence of triethyl amine, and finally by a base-induced
de-O-acetylation.
Scheme 2. Synthesis of 2-(3,4-dihydroxyphenyl) acetic acid esters.
RO
RO
OH
()
ii
RO
RO
O
n
O
O
10; R = H
12-13; n = 1, 2; R = Ac
14-15; n = 1, 2; R = H
i
iii
11; R = Ac
Reagents and conditions: (i) Ac2O, H2SO4, Et2O, rt; (ii) SOCl2, DMF, HO(CH2)2Ph or HO(CH2)3Ph,
Et3N, CH2Cl2, rt; (iii) guanidine·HCl, Et3N, CH2Cl2, MeOH, rt.
Commercially available 3,4-dihydroxybenzoic acid (3,4-DHB, 16) was used for the synthesis of
caffeic acid ester analogs 20, 21 in which no carbon separates the carbonyl group from the catechol
moiety. The same strategy for the synthesis of 14 and 15 is used for the preparation of these esters
(Scheme 3).
Scheme 3. Synthesis of 3,4-dihydroxybenzoic acid esters.
O
O
ii
RO
RO
RO
RO
( )
OH
O
n
18-19; n = 1, 2; R = Ac
20-21; n = 1, 2; R = H
16, R = H
iii
i
17, R = Ac
Reagents and conditions: (i) Ac2O, H2SO4, Et2O, rt; (ii) SOCl2, DMF, HO(CH2)2Ph or HO(CH2)3Ph,
Et3N, CH2Cl2, rt; (iii) guanidine·HCl, Et3N, CH2Cl2, MeOH, rt.

Molecules 2012, 17
14641
2.2. Free Radical Scavenging Activity
The DPPH assay was used to assess the free radical scavenging activity of our synthesized
compounds. Namely we investigated their capacity to block the formation of the purple DPPH radical
(DPPH.) by reducing these radicals to the corresponding yellow hydrazine. Special attention was
required for the preparation of the control (DPPH reagent + ethanol without test compounds). The
antiradical activities of all compounds are shown in Table 1. All of the IC50 are calculated relative to
the control. Magalhaes et al. have shown that in this case the percentage of radical scavenged is
dependent on the initial concentration of the radical DPPH [26]. All of the tested compounds
incorporated basic structural features favoring antioxidant activity: catechol groups/hydroxyl groups
and the presence of carbonyl groups. In this study we tried to evaluate the effect of other structural
parameters present in caffeic acid/CAPE: the ethylene moiety, the length of the linker attaching the
carbonyl to the catechol moiety and the length of the linker between the phenethyl group and the
carbonyl. It appears that for a certain length of the linker between the catechol group and the carbonyl
(2C with a double bond, an ethylene moiety) the free radical scavenging activity is better. Caffeic acid
(1), CAPE (5) and 6 all bear an ethylene moiety and are more active (IC50 = 10–16 µM) at scavenging
radicals than their counterparts 7 and 8 (IC50 = 23–25 µM) lacking the double bond but still retaining
the 2C between the carbonyl and the catechol ring, so the ethylene moiety is important, but not a
determining feature dictating radical scavenging activity, as illustrated by 3,4-DOPAC 10 and
dihydrocaffeic acid (9) which, despite lacking the ethylene moiety, are the most active of the tested
compounds (IC50 = 7–8 µM). While assessing the contribution of the ethylene link in antioxidant
activity, Jayaprakasam and co-workers obtained similar results by showing that dihydrocaffeic acid
which lacks the ethylene link was more active than caffeic acid itself [16].
Table 1. Free radical scavenging activity of test compounds.
Compound
IC50 (μM)
15.3
16.5
11.9
7.8
Compound
IC50 (μM)
7.1
1
5
6
9
7
8
10
14
15
16
20
21
18.1
20.3
43.7
24.6
23
20.4
9.6
Direct attachment of the carbonyl group on the catechol ring negates or decreases radical
scavenging activities as reported earlier by other groups [27]. DHB 16, whose carbonyl group is
directly linked to the aromatic ring, has the lowest free radical scavenging activity (IC50 = 44 µM) of
all the tested compounds. By comparison 3,4-DOPAC 10, whose carbonyl has been moved one C
away from the aromatic ring, is much more potent (IC50 = 7 µM). A further increase to 2 C atoms
away from the aromatic ring doesn’t bring about any significant change (hyCaf Ac (9): IC50 = 7.8 µM).
As to the influence of the link between the carbonyl and the phenethyl, the patterns are less obvious.
The analogues DHB (compound 16), 20 and 21 all lack the ethylene moiety and their carbonyl is
directly linked to the catechol ring. In this particular case DHB 16 still showed poor antiradical
activity. Compounds 20 and 21 showcasing a phenyl group separated from the carbonyl by a linker of

Molecules 2012, 17
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2 and 3 C atoms, respectively, were much more potent. Lengthening the linker between phenethyl and
carbonyl from 2 C (compound 20) to 3 C atoms (compound 21) increased the activity by almost two-fold.
It appears that the ethylene group gains significance when there are 1 to 2 C atoms between the
carbonyl and the catechol. Thus compounds 7, 8, 14 and 15 lacking the ethylene are less active at
scavenging radicals than CAPE (5) and compound 6 which contain the ethylene moiety. In such a case
the presence of the phenethyl group seems to be less relevant as illustrated by the similar IC50 of CAPE
(5) and caffeic acid (1). They both have the ethylene moiety but CAPE (5) also has a phenethyl group.
The influence of the phenethyl group is more important when the carbonyl is directly linked to the
catechol ring. Based on these results it seems that the most potent radical scavengers in this series of
CAPE (5) analogues are molecules bearing catechol rings and a carbonyl group separated from the
aromatic ring by 1–2 C atoms.
2.3. Antioxidant Activity
Antioxidant activity mainly involves two major mechanisms: electron transfer (ET) and hydrogen
atom transfer (HAT). Thus it is of interest to evaluate which one of these mechanisms is favored by
our test compounds. Carotenoids are relatively poor quenchers of peroxyl radicals and are
exceptionally active at quenching singlet oxygen, whereas phenolic compounds are active against
peroxyl radicals and ineffective against singlet oxygen [21]. Among the effects produced in vivo by
radicals, lipid peroxidation is a serious one. Lipid peroxides resulting from radical action can alter the
membrane fluidity and modify the function of membrane proteins. In turn these lipid peroxides can
generate peroxyl radicals leading to toxic end-products such as malondialdehyde [22].
Peroxyl (ROO•) scavenging activity assesses the capacity of an antioxidant to quench these radicals
by the HAT mechanism. The most used peroxyl radical generators are the water-soluble 2,2-azobis(2-
amidinopropane) dihydrochloride (AAPH) and the lipid-soluble 2,2-azobis(2,4-dimethylvaleronitrile)
(AMVN). In the emulsion-based AAPH assay, the presence of antioxidant inhibits or slows down the
oxidation of linoleic acid induced by peroxyl radicals [22]. The observed data on the antioxidant
activity of all compounds are shown in Table 2.
Table 2. Antioxidant activity of test compounds.
Compound
IC50 (μM)
2.01
Compound
IC50 (μM)
3.29
1
5
6
9
7
8
10
14
15
16
20
21
1.09
3.00
3.94
3.80
2.10
9.10
0.70
1.20
2.19
1.83
As previous results have shown [28], there is no direct correlation between the results from the
DPPH assay and those from the AAPH assay. Compound 7 is the most potent of the tested compounds
at inhibiting lipid peroxidation with an IC50 of 0.70 µM. In comparison, its radical scavenging
potential is one of the weakest with an IC50 of 24.6 µM (Table 1). As for the structural patterns
dictating the protective effect against lipid peroxidation, one feature is apparent. The simultaneous

Molecules 2012, 17
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absence of the ethylene moiety and the presence of a direct link of the carboxyl on the aromatic ring
generates compounds with low antioxidant activity such as illustrated by DHB (16, IC50 = 9.10 µM). A
consistent decrease of antioxidant activity is reported with derivatives of benzoic acid where the
carbonyl is directly linked to the aromatic ring compared to derivatives of cinnamic acid [15]. The
importance of the phenethyl ring has been conclusively demonstrated in the case of NF-κB inhibition
by Lee and coworkers [29]. The most active compound among the CAPE analogues used in that study
was the one bearing the phenethyl group [29].
Spacing the carboxyl with one C atom induced a 3-fold increase in potency as shown with DOPAC
(compound 10, IC50 = 3.29 µM). Also the presence of an ester group (phenethyl/phenpropionyl) has
similar effects even when the carbonyl is directly linked to the aromatic ring. Compounds 20 and 21
with respective IC50 values of 1.2 and 1.83 µM show a 4-fold increase in potency compared to DHB
(compound 16), even if their carbonyl group is linked directly to the catechol ring.
The presence of the ethylene moiety is not a mandatory requisite for antioxidant activity. Caffeic
acid (1) and its dehydrogenated counterpart dihydrocaffeic acid (9) have similar IC50 values: 2.01 and
2.10, respectively. This feature is also illustrated by the pairs CAPE (5) and 7 (IC50 = 1.09 and 0.70,
respectively) and compounds 6 and 7 (IC50 = 3.94 and 2.19, respectively). Increasing the length of the
linker by 1 C atom between the non-catechol aromatic ring and the carbonyl group consistently
decreases the antioxidant activity. Compounds with an ethyl linker such as CAPE (5), 7, 14 and 20
(IC50 = 1.09, 0.70, 3, 1.2 respectively) have better activities than their parent compounds with a propyl
linker, namely 6, 8, 15 and 21 (IC50 = 3.94, 2.19, 3.80, 1.83 respectively).
3. Experimental
3.1. General
All chemicals used were purchased from Aldrich. Purification of compounds was carried out by
silica gel circular chromatography (Chromatotron®, model 7924, Harrison Research, Palo Alto, CA,
USA). Thin layer chromatography (TLC) was run on silica gel coated aluminum sheets (SiliaPlate
TLC, Silicycle®) with detection by UV light (254 nm, UVS-11, Mineralight® shortwave UV lamp).
Melting points were obtained using a MEL-TEMP® (model 1001D) melting point apparatus. FTIR
spectra were recorded on a Nicolet® Impact 400 spectrometer. NMR spectra were recorded on a Bruker®
Avance III 400 MHz spectrometer. High resolution mass measurements were performed on a Bruker®
Doltonics’ micrOTOF instrument in positive or negative electrospray.
3.2. Synthesis
(E)-3-Phenylpropyl-3-(3,4-Diacetoxyphenyl)acrylate (4). A mixture of diacetylcaffeic acid (2, 300 mg,
1.13 mmol), thionyl chloride (5 mL) and two drops of DMF was heated at reflux for 4 h. The
excess thionyl chloride (SOCl2) was removed on a rotovap, and the residue was dissolved in dry
CH2Cl2 (4 mL). To this solution was slowly added pyridine (1 mL) and 3-phenylpropan-1-ol (232.0 μL,
1.71 mmol, 1.3 eq.). The resulting mixture was stirred overnight at room temperature. After
removal of solvents, the residue was dissolved in dichloromethane (25 mL), the organic extract
was washed with water (2 × 20 mL), brine (2 × 20 mL), and then dried over MgSO4. The resulting

Molecules 2012, 17
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residue was purified by silica gel circular chromatography using 5–15% EtOAc-hex to afford 314 mg
(yield = 73%) of the desired derivative 4 as a white solid. M.p. = 66–67 °C; Rf = 0.60 (30%
1
EtOAc–hex); H-NMR (CDCl3, 25 °C); δ (ppm): 7.63 (d, J = 16.01 Hz, 1H, =CHCar), 7.45–7.21
(m, 8H, Har), 6.41 (d, 15.97 Hz, 1H, =CHCO), 4.25 (t, J = 6.52 Hz, 2H, CH2(CH2)2Ph), 2.77 (t,
J = 7.44 Hz, 2H, (CH2)2CH2Ph), 2.33 (s, 6H, 2 × OAc), 2.06 (quint., J = 6.52 Hz, 2H,
CH2CH2CH2Ph); 13C-NMR (CDCl3, 25 °C); δ (ppm): 168.08, 168.00, 166.60, 143.48, 142.76,
142.45, 141.20, 133.33, 128.47, 128.44, 126.41, 126.03, 123.93, 122.73, 119.34, 64.06, 32.26,
30.27, 20.66, 20.63; HRMS m/z calc. for C22H22O6 + (Na+) : 405.1309; found: 405.1311.
(E)-3-Phenylpropyl-3-(3,4-dihydroxyphenyl)acrylate (6). To a solution of 4 (165.81 mg, 0.43 mmol) in
a 1:1 mixture of MeOH and CH2Cl2 (5 mL) was added guanidine·HCl (123 mg, 1.29 mmol, 1.5 eq. per
OAc). The reaction mixture was stirred for 2 h. After removal of solvents, the residue was dissolved in
EtOAc (25 mL), washed with saturated NH4Cl solution, with brine and dried over MgSO4. After
filtration and evaporation of the solvent, pure deprotected 6 (123 mg, 93%) was obtained as a yellow
solid. M.p. = 116–118 °C; Rf = 0.46 (5% MeOH–CH2Cl2); 1H-NMR (DMSO-d6, 25 °C): δ (ppm): 7.47
(d, J = 15.89 Hz, 1H, =CHCar), 7.31–7.18 (m, 5H, Har), 7.06–7.00 (m, 2H, Har), 6.77 (d, J = 8.08 Hz, 1H,
Har), 6.28 (d, 15.89 Hz, 1H, =CHCO), 4.11 (t, J = 6.28 Hz, 2H, CH2(CH2)2Ph), 2.68 (t, J = 7.36 Hz,
13
2H, (CH2)2CH2Ph), 1.96–1.91 (m, 2H, CH2CH2CH2Ph); C-NMR (CDCl3, 25 °C) δ (ppm): 168.11,
168.02, 166.61, 143.46, 142.77, 142.43, 141.21, 133.33, 128.47, 128.45, 126.43, 126.04, 123.94,
122.73, 119.33, 64.06, 32.25, 30.27, 20.68, 20.65; HRMS m/z calc. for C18H18O4 + (Na+): 321.1097;
found: 321.1083.
Phenethyl-3-(3,4-dihydroxyphenyl)propanoate (7). Compound 5 (152 mg, 0.53 mmol) was dissolved
in MeOH (10 mL) and 10% Pd/C (16 mg) was added. The flask was sealed with a rubber septum and
positive pressure of H2 was maintained by a balloon attached via a syringe needle. The progress of the
reaction was monitored by TLC until the complete conversion after 16 h. The reaction mixture was
filtered through celite and the solvent was removed under reduced pressure to give pure 7 (150 mg,
1
quantitative yield) of a colorless oil. Rf: 0.23 (30% EtOAc–hex); H-NMR (CDCl3, 25 °C); δ (ppm):
7.34–7.21 (m, 5H, Har), 6.77 (d, J = 8.00 Hz, 1H, Har), 6.66 (s, 1H, Har), 6.59 (d, J = 8.00 Hz, 1H, Har),
4.31 (t, J = 7.00 Hz, 2H, CH2CH2Ph), 2.94 (t, J = 6.96 Hz, 2H, CH2CH2Ph)), 2.82 (t, J = 7.52 Hz, 2H,
13
CarCH2CH2C(=O)), 2.59 (t, J = 7.68 Hz, 2H, CarCH2CH2C(=O)); C-NMR (CDCl3, 25 °C); δ (ppm):
173.49, 143.59, 142.08, 137.78, 133.25, 128.93, 128.52, 126.60, 120.57, 115.37, 65.16, 36.15, 35.04,
30.24; HRMS m/z calc. for C17H18O4 + (Na+): 309.1097; found: 309.1083.
3-Phenylpropyl-3-(3,4-dihydroxyphenyl)propanoate (8). Compound 8 was prepared from 6 (112 mg,
0.37 mmol) and 10% Pd/C (12 mg) following the same protocol as for 7 which gave 8 (110 mg,
quantitative yield) as a yellow oil; Rf: 0.76 (30% EtOAc–hexanes); 1H-NMR (CDCl3, 25 °C); δ (ppm):
7.31–7.15 (m, 5H, Har), 6.79–6.76 (m, 2H, Har), 6.58 (d, J = 6.72 Hz, 1H, Har), 4.08 (t, J = 6.09 Hz, 2H,
CH2(CH2)2Ph), 2.78 (m, 2H, CarCH2CH2C(=O)), 2.66–2.54 (m, 4H, CarCH2CH2C(=O), (CH2)2CH2Ph)),
1.96–1.91 (m, 2H, CH2CH2CH2Ph); 13C-NMR (CDCl3, 25 °C); δ (ppm): 173.68, 143.26, 141.69,
141.12, 133.52, 128.45, 128.38, 126.02, 120.74, 115.44, 64.16, 36.03, 32.09, 30.22, 30.07; HRMS m/z
calc. for C18H20O4 + (Na+): 323.1254; found: 323.1261.

Molecules 2012, 17
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2-(3,4-Diacetoxyphenyl)acetic acid (11). In a 10-mL round-bottom flask, 2-(3,4-dihydroxyphenyl)
acetic acid (10, 496 mg, 2.95 mmol) was dissolved in acetic anhydride (3.5 mL) and sulfuric acid
(0.1 mL) with stirring. The reaction mixture was stirred for 5 min and then ether (5 mL) was added.
The solution was stirred for 24 h under argon. Subsequently, the mixture was poured into ice water
(50 mL), extracted with EtOAc (50 mL), dried over MgSO4 and charcoal, filtered and concentrated.
After recrystallization from EtOAc–hex (3:2), 2-(3,4-diacetyloxy)phenyl) acetic acid (11, 507 mg,
1
68%) was obtained as a white solid. M.p. = 104–106 °C; Rf = 0.37 (5% EtOAc-hex); H-NMR
(CDCl3, 25 °C); δ (ppm): 7.22–7.16 (m, 3H, Har), 3.66 (s, 2H, CH2), 2.31 (s, 6H, 2 × OAc); 13C-NMR
(CDCl3, 25 °C); δ (ppm): 176.41, 168.25, 168.22, 142.00, 141.36, 131.88, 127.62, 124.47, 123.50,
40.18, 20.65, 20.63; HRMS m/z calc. for C12H12O6 (H+): 251.0561; found: 251.0565.
Phenethyl-2-(3,4-diacetoxyphenyl)acetate (12). Compound 12 was prepared from 11 (478 mg, 1.9 mmol),
SOCl2 (12 mL), 2-phenylethan-1-ol (296 μL, 2.47 mmol), and pyridine (170 μL, 2.10 mmol) using the
procedure for the synthesis of 4. Purification by silica gel circular chromatography (5%–10%
EtOAc–hex) gave 12 (467 mg, 69%) as a yellow oil. Rf = 0.36 (5% EtOAc-hex); 1H-NMR (400 MHz,
CDCl3, 25 °C); δ (ppm): 7.33–7.25 (m, 4H, Har), 7.19–7.18 (m, 2H, Har), 7.14 (m, 2H, Har), 4.34 (t,
J = 6.96 Hz, 2H, CH2CH2Ph), 3.60 (s, 2H, CarCH2CO), 2.95 (t, J = 6.96 Hz, 2H, CH2CH2Ph), 2.31 (s,
6H, 2 × OAc); 13C-NMR (101 MHz, CDCl3, 25 °C); δ (ppm): 170.68, 168.22, 168.14, 141.94, 141.17,
137.63, 132.62, 128.91, 128.50, 127.48, 126.56, 124.34, 123.38, 65.51, 40.65, 35.00, 20.66, 20.64;
HRMS m/z calc. for C20H20O6 + (Na+): 379.1152; found: 379.1137.
3-Phenylpropyl-2-(3,4-diacetoxyphenyl)acetate (13). Compound 13 was prepared from 11 (500 mg,
1.9 mmol), SOCl2 (12 mL), 3-phenylpropan-1-ol (360 μL, 2.65 mmol), and pyridine (170 μL, 2.10 mmol)
using the procedure for the synthesis of 4. Purification by silica gel circular chromatography (5%–12%
1
EtOAc–hex) gave 13 (491 mg, 67%) as a yellow oil. Rf = 0.64 (30% EtOAc-hex); H-NMR (CDCl3,
25 °C); δ (ppm): 7.34–7.30 (m, 2H, Har), 7.25–7.18 (m, 6H, Har), 4.15 (t, J = 6.48 Hz, 2H,
CH2(CH2)2Ph), 3.63 (s, 2H, CarCH2CO), 2.69 (t, J = 7.52 Hz, 2H, (CH2)2CH2Ph), 2.31 (s, 6H,
2 × OAc), 1.99 (quint., J = 6.60 Hz, 2H, CH2CH2CH2Ph); 13C-NMR (CDCl3, 25 °C): δ (ppm): 170.83,
168.23, 168.16, 142.03, 141.24, 141.13, 132.81, 128.57, 128.48, 128.45, 128.41, 127.48, 126.05,
124.37, 123.43, 64.40, 40.66, 32.12, 30.12, 20.64, 20.63; HRMS m/z calc. for C21H22O6 + (Na+):
393.1309; found: 393.1321.
Phenethyl-2-(3,4-dihydroxyphenyl)acetate (14). Compound 14 was prepared from 12 (205 mg, 0.57 mmol)
and guanidine·HCl (183 mg, 1.9 mmol) following the same protocol as for 6. Purification by silica gel
circular chromatography (3%–10% EtOAc–hex) gave 14 (98 mg, 63%) as a yellow oil. Rf = 0.52 (5%
1
MeOH–CH2Cl2); H-NMR (MeOD, 25 °C); δ (ppm): 7.27–7.14 (m, 5H, Har), 6.72–6.70 (m, 2H, Har),
6.54 (dd, J = 8.04 Hz, 1.76 Hz, 1H, Har), 4.27 (t, J = 6.80 Hz, CH2CH2Ph), 3.44 (s, 2H, CarCH2CO),
13
2.89 (t, J = 6.76 Hz, 2H, CH2CH2Ph); C-NMR (MeOD, 25 °C); δ (ppm): 172.56, 144.91, 144.06,
137.91, 128.59, 128.04, 126.05, 125.51, 120.28, 116.04, 114.92, 65.13, 40.14, 34.60; HRMS m/z calc.
for C16H16O4 + (Na+): 295.0941; found: 295.0932.
3-Phenylpropyl-2-(3,4-dihydroxyphenyl)acetate (15). Compound 15 was prepared from 13 (295 mg,
0.79 mmol), guanidine·HCl (254 mg, 2.66 mmol), and Et3N (1.1 mL) following the same protocol as

Molecules 2012, 17
14646
for 6. Purification by silica gel circular chromatography (5%–8% EtOAc–hex) gave 15 (136 mg, 60%)
as a yellow oil. Rf = 0.47 (5% MeOH–CH2Cl2); 1H-NMR (MeOD, 25 °C); δ (ppm): 7.27–7.23 (m, 2H,
Har), 7.18–7.11 (m, 3H, Har), 6.76–6.72 (m, 2H, Har), 6.62 (dd, J = 8.08 Hz, 1.96 Hz, 1H, Har), 4.06
(t, J = 6.32 Hz, 2H, CH2(CH2)3Ph), 3.47 (s, 2H, CarCH2CO), 2.63 (t, J = 7.44 Hz, 2H, (CH2)3CH2Ph),
1.92 (quint., J = 6.44 Hz, 4H, CH2(CH2)2CH2Ph); 13C-NMR (MeOD, 25 °C); δ (ppm): 172.70, 145.00,
144.30, 141.14, 128.08, 127.99, 125.68, 125.52, 120.23, 115.95, 114.92, 53.56, 40.23, 31.54, 30.05;
HRMS m/z calc. for C17H18O4 + (Na+): 309.1097; found: 309.1085.
3,4-Diacetoxybenzoic acid (17). Compound 17 was prepared from 3,4-dihydroxybenzoic acid (DHB,
16, 1 g, 6.52 mmol), acetic anhydride (6.5 mL), sulfuric acid (0.1 mL), and ether (20 mL) following
the same protocol as for 11. Recrystallization from EtOAc–hex (3:2), acid 3,4-bis(acetyloxy)benzoic
acid (17, 1.3 g, 83%) was obtained as a white solid. M.p. = 158–160 °C; Rf = 0.32 (30% EtOAc–hex);
1H-NMR (CDCl3, 25 °C): δ (ppm): 11.42 (s large, 1H, OH), 8.05 (dd, J = 8.48 Hz, 1.88 Hz, 1H, Har),
7.97 (d, J = 1.84 Hz, 1H, Har), 7.35 (d, J = 8.48 Hz, 1H, Har), 2.35 (s, 6H, 2 × OAc); 13C-NMR (CDCl3,
25 °C); δ (ppm): 170.32, 167.97, 167.63, 146.73, 142.10, 128.78, 127.77, 125.71, 123.68, 20.69,
20.56; HRMS m/z calc. for C11H10O6 (H+): 237.0405; found: 237.0404.
Phenethyl-3,4-diacetoxybenzoate (18). Compound 18 was prepared from 17 (505 mg, 2.1 mmol),
SOCl2 (12 mL), 2-phenylethan-1-ol (340 μL, 2.84 mmol), and pyridine (200 μL, 2.47 mmol) using the
procedure for the synthesis of 4. Purification by silica gel circular chromatography (5%–10%
EtOAc–hex) gave 18 (486 mg, 67%) as a yellow oil. Rf = 0.52 (30% EtOAc–hex); 1H-NMR (CDCl3, 25 °C):
δ (ppm): 7.92–7.88 (m, 2H, Har), 7.38–7.31 (m, 3H, Har), 7.28–7.25 (m, 3H, Har) 4.32 (t, J = 6.5 Hz,
CH2CH2Ph), 2.78 (t, J = 7.7 Hz, 2H, CH2CH2Ph), 2.32 (s, 6H, 2 × OAc); 13C-NMR (CDCl3, 25 °C); δ
(ppm): 168.01, 167.83, 146.82, 143.01, 140.12, 128.84, 128.71, 128.36, 128.06, 126.12, 125.02,
123.65, 64.78, 34.41, 20.72, 20.43; HRMS m/z calc. for C19H18O6 + (Na+): 365.0996; found: 365.0996.
3-Phenylpropyl-3,4-diacetoxybenzoate (19). Compound 19 was prepared from 17 (500 mg, 2.1 mmol),
SOCl2 (15 mL), 3-phenylpropan-1-ol (380 μL, 2.79 mmol), and pyridine (180 μL, 2.23 mmol) using
the procedure for the synthesis of 4. Purification by silica gel circular chromatography (1%–18%
1
EtOAc–hex) gave 19 (493 mg, 66%) as a yellow oil. Rf = 0.48 (30% EtOAc–hex); H-NMR (CDCl3,
25 °C); δ (ppm): 7.95 (dd, J = 8.44, 2 Hz, 1H, Har), 7.86 (d, J = 2 Hz, 1H, Har), 7.31–7.28 (m, 3H, Har),
7.24–7.22 (m, 3H, Har) 4.36 (t, J = 6.5 Hz, CH2CH2CH2Ph), 2.80 (t, J = 7.8 Hz, 2H, CH2CH2CH2Ph),
13
2.34 (s, 6H, 2 × OAc), 2.12 (quint., J = 6.5 Hz, 2H, CH2CH2CH2Ph); C-NMR (CDCl3, 25 °C); δ
(ppm): 168.03, 167.72, 145.94, 141.98, 141.07, 128.97, 128.50, 128.44, 128.11, 126.07, 124.99,
123.49, 64.71, 32.29, 30.19, 20.69, 20.59; HRMS m/z calc. for C20H20O6 + (Na+): 379.1152; found:
379.1134.
Phenethyl-3,4-dihydroxybenzoate (20). Compound 20 was prepared from 18 (250 mg, 0.73 mmol),
guanidine·HCl (246 mg, 2.57 mmol), and Et3N (1.1 mL) following the same protocol as for 6.
Purification by silica gel circular chromatography (5%–10% EtOAc–hex) gave 20 (170 mg, 90%) as a
yellow solid. M.p. = 128–130 °C; Rf = 0.82 (5% MeOH–CH2Cl2); 1H-NMR (MeOD, 25 °C); δ (ppm):
7.42–7.39 (m, 2H, Har), 7.31–7.30 (m, 4H, Har), 7.25–7.19 (m, 1H, Har), 6.80 (d, J = 8.12 Hz, 1H, Har),
13
4.47–4.43 (m, 2H, CH2CH2Ph), 3.07–3.02 (m, 2H, CH2CH2Ph); C-NMR (MeOD, 25 °C); δ (ppm):

Molecules 2012, 17
14647
166.85, 150.32, 144.76, 138.14, 128.60, 128.11, 126.12, 122.22, 121.30, 116.00, 114.42, 65.01, 34.83;
HRMS m/z calc. for C15H14O4 + (Na+): 281.0784; found: 281.0774.
3-Phenylpropyl-3,4-dihydroxybenzoate (21). Compound 21 was prepared from 19 (150 mg, 0.42 mmol),
guanidine·HCl (133 mg, 1.4 mmol), and Et3N (578 μL) following the same protocol as for 6.
Purification by silica gel circular chromatography (5%–10% EtOAc–hex) gave 21 (103 mg, 90%) as a
yellow solid. M.p. = 125–126 °C; Rf = 0.7 (5% MeOH–CH2Cl2); 1H-NMR (DMSO-d6, 25 °C); δ (ppm):
7.41–7.39 (m, 1H, Har), 7.35–7.27 (m, 3H, Har), 7.24–7.17 (m, 3H, Har), 6.83 (d, J = 8.2 Hz, 1H, Har),
4.17 (t, J = 6.4 Hz, 2H, CH2CH2CH2Ph), 2.71 (t, J = 7.5 Hz, 2H, CH2CH2CH2Ph), 1.98 (quint.,
J = 6.4 Hz, 2H, CH2CH2CH2Ph); 13C-NMR (DMSO-d6, 25 °C); δ (ppm): 166.15, 150.88, 145.53,
141.63, 128.82, 128.78, 126.34, 122.27, 121.16, 116.74, 115.78, 63.75, 32.0, 30.36; HRMS m/z calc.
for C16H16O4 + (Na+): 295.0941; found : 295.0935.
3.3. In Vitro Antioxidant Activity
3.3.1. AAPH Assay
The antioxidant assay was performed as previously described by Liégeois and al. [30]. Briefly, a
5 mM phosphate-buffered solution (pH 7.4) containing 0.05% Tween 20 (Sigma-Aldrich) and
0.16 mM linoleic acid (Cayman Chemical, Ann Arbor, MI, USA) was preheated at 40 °C. Test
compounds or their diluent (DMSO) were added to the mix at the indicated concentrations. The
oxidation reaction, performed under a constant temperature of 37 °C, was initiated with the addition of
50 µL of 2,2'-azobis(2-amidinopropane) dihydrochloride (AAPH) solution (10 mg·mL−1) (Cayman
Chemical) to 1 mL of the above solution. The rate of lipid oxidation was determined by measuring the
absorbance at 234 nm with a Thermo Varioskan UV visible spectrophotometer at every 5 min for 3 h.
Inhibition of linoleic acid oxidation was calculated as follows: (%) = (1 − rate absorbance change with
test compound/rate of absorbance change with solvent control) × 100.
3.3.2. DPPH Assay
The radical scavenging activity of test compounds was measured as previously described using
2,2-diphenyl-1-picrylhydrazyl (DPPH) as a stable radical [31] with slight modifications. Particular
care was taken in the preparation of the control (DPPH reagent + ethanol as a diluent without test
compounds). Controls with O.D. of 0.350–0.360 at 520 nm were deemed as acceptable to avoid
variations in IC50 calculations. DPPH in ethanol (1 mL, 60 mM) was mixed with the test compounds
(1 mL) at the indicated concentrations or their diluent (ethanol). Each mixture was then shaken
vigorously and held in the dark for 30 min at room temperature. The absorbance of DPPH at 520 nm
was then measured. The radical scavenging activity was expressed in terms of % inhibition of DPPH
absorbance:
% Inhibition = [(Acontrol − Atest)/Acontrol)] × 100
where Acontrol is the absorbance of the control (DPPH solution without test compound) and Atest is the
absorbance of the test sample (DPPH solution plus compound).

Molecules 2012, 17
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3.3.3. Data Analysis
All data are expressed as means of two experiments; each experiment being performed in triplicate.
IC50 values were calculated from a sigmoidal concentration-response curve-fitting model with a
variable slope on GraphPad Prism 5 software (GraphPad Software, San Diego, CA, USA).
4. Conclusions
Structural modifications of the CAPE (5) core have shown the possibility to synthesize molecules
or analogues with improved antioxidant/radical scavenging properties when compared to CAPE (5).
Well-known structural prerequisites include the presence of a catechol ring and a short spacer between
the catechol and the carbonyl moiety. In our series of CAPE (5) analogues, the presence of the
ethylene moiety was important, but not a determining factor for radical scavenging using an ET
mechanism while in a HAT type mechanism (AAPH assay), its presence mattered less. As to the
importance of the linker between the phenyl and the carbonyl, it appears that the ethyl promoted better
antioxidant activity compared to the propionyl group.
Acknowledgments
This research was financially supported by the New Brunswick Health Research Foundation, the
Canada Foundation for Innovation, the New Brunswick Innovation Foundation, the Canada Research
Chairs program and Université de Moncton. A.P. and M.H. thank the New Brunswick Health Research
Foundation for fellowship support.
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Sample Availability: Samples of the compounds 5–8, 14, 15, 20, 21 are available from the authors.
© 2012 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article
distributed under the terms and conditions of the Creative Commons Attribution license
(http://creativecommons.org/licenses/by/3.0/).