An efficient chemoselective reduction of furan series unsaturated dinitriles

Article abstract of DOI:10.3390/molecules18022212

An efficient reduction of double bonds conjugated with nitrile groups and acid or base sensitive furan rings with 2-phenylbenzimidazoline generated in situ has been successfully accomplished with high yields and excellent selectivity. The employed reducin

Full text of DOI:10.3390/molecules18022212

Molecules 2013, 18, 2212-2221; doi:10.3390/molecules18022212
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molecules
ISSN 1420-3049
www.mdpi.com/journal/molecules
Article
An Efficient Chemoselective Reduction of Furan Series
Unsaturated Dinitriles
Pavel Bobal 1,* and Janette Bobalova 2
1
Department of Chemical Drugs, Faculty of Pharmacy, University of Veterinary and
Pharmaceutical Sciences Brno, Palackeho 1/3, 612 42 Brno, Czech Republic
2
Institute of Analytical Chemistry of the Academy of Sciences of the Czech Republic, v. v. i.,
Veveří 97, 602 00 Brno, Czech Republic
* Author to whom correspondence should be addressed; E-Mail: bobalp@vfu.cz;
Tel.: +420-54156-2927; Fax: +420-54124-0607.
Received: 14 December 2012; in revised form: 28 January 2013 / Accepted: 30 January 2013 /
Published: 11 February 2013
Abstract: An efficient reduction of double bonds conjugated with nitrile groups and acid
or base sensitive furan rings with 2-phenylbenzimidazoline generated in situ has been
successfully accomplished with high yields and excellent selectivity. The employed
reducing agent was prepared in one step from ordinary chemicals. The other advantages of
the presented method include mild and convenient reaction conditions, a benign and cost
effective reagent, simple work-up and separation of the products. As this process does
neither affect cyano and nitro groups nor furan rings, it is a valuable alternative when
metal-catalyzed hydrogenations or borohydride reductions have failed.
Keywords: chemoselective reduction; regioselective reduction; conjugated olefins;
organic hydride compounds; furan ethylenes; unsaturated dinitriles; 2-
phenylbenzimidazoline
1. Introduction
Substituted furans are important and ubiquitous structural units present in large number of natural
compounds [1], pharmaceuticals [1,2] and have been widely used as synthetic building blocks for the
synthesis of many organic materials [3,4]. Their synthesis, however, still remains a challenge for
synthetic chemists. The chemoselective reduction of conjugated double bonds with a furan nucleus

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constitutes a rather troublesome case, as a consequence of the ease of saturation of the heterocyclic
moiety [5,6], and the well-known sensitivity of furans to either acids or bases [7,8].
Further, the reduction of substituted propenenitriles to saturated propanenitriles often proceeds with
concomitant reduction of the nitrile moiety, polymerization and other side reactions [9]. At present,
numerous methods for the reduction of unsaturated nitriles have been developed, including catalytic
hydrogenation [10], reductions with organostannic hydrides [11,12], formic acid-triethylamine
azeotrope [13], magnesium in methanol [9], sodium borohydride [14,15], sodium cyanoborohydride [16],
and many others. Despite the fact that a large group of reducing agents are used for reduction of
conjugated unsaturated nitriles, only a limited number might be considered as really selective and
accepted as being synthetically useful. To this group belong the so called organic hydride compounds.
They can transfer hydrogen to the substrates in the form of hydride anions [17]. These hydride donors
are well known in different forms in nature, such as NADH, FADH2 and others. In recent years, many
biomimetic organic hydride compounds were synthesized mainly containing six-membered heterocyclic
systems like Hantzsch esters possessing 1,4-dihydropyridine as a redox active centre [18–21]. The
other group of heterocyclic compounds having hydrogen-donating ability is a group of five-membered
heterocycles, such as dihydrobenzazoles and their usefulness as selective reducing agents has been
shown [22–25]. Finally N,N,N',N',N'',N''-hexaethylphosphorous triamide was also successfully used
for the reduction of 3-(furan-2-yl)-2-cyanopropenenitrile and its thiophene analog [26].
2. Results and Discussion
2.1. Chemistry
The selective reduction of conjugated C=C bonds with strong electron-withdrawing groups like
cyano, nitro or carbonyl groups has been one of the most desirable transformations in organic
chemistry. Chemoselective reductions of unsaturated nitriles have attracted much attention for several
decades because the reduction products were very important intermediates in organic synthesis.
The goal of the study was to find a suitable method for the chemoselective reduction of 3-phenyl,
3-(thiophen-2-yl) and 3-(5-substituted furan-2-yl)-2-cyanopropenenitriles 1a–g. The products of the
reaction e.g. aryl and heteroarylmethylpropanedinitriles, are important intermediates for the synthesis
of many biologically active heterocyclic compounds [27].
The substrates for the reduction reaction, 3-phenyl, 3-(thiophen-2-yl) and 3-(5-substituted furan-2-
yl)-2-cyanopropenenitriles 1a–g, were easily synthesized from the corresponding aldehydes and
propanedinitrile, via Knoevenagel condensation catalyzed with piperidine in ethanol [28,29] according
to Scheme 1. The 5-substituted furan-2-carbaldehydes starting materials were prepared according to
procedures described earlier [30–32].
The reduction of 3-aryl-2-cyanopropenenitriles is well established [9–16,18–25,33–36]. A large
numbers of processes have been developed for this purpose, among which the most important are
catalytic hydrogenation [33,34] and borohydride reduction [35,36]. We have initially started with an
investigation of these methods and their application to substituted furan derivatives. In our hands,
reduction of 3-phenyl-2-cyanopropenenitrile (1a) with sodium borohydride in methanol worked well
and we isolated 2-benzylpropanedinitrile (3a) [37] in 85% yield. When applied to 3-(thiophen-2-yl)-2-
cyanopropenenitrile (1b), the result was rather similar. Borohydride reduction of 3-(furan-2-yl)-2-

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cyanopropenenitrile (1c) also afforded product 3c [38] in a satisfactory 61% yield. The problem arose
when this method of reduction was employed for 5-substituted furan olefins 1d–g. In case of
5-bromoderivative 1d the formation of many side products was observed. Utilization of this process
for 5-nitro, 5-phenylsulfanyl and 5-tosylderivatives 1e–g only led to decomposition within a short time
and there was no sign of formation of the desired products 3e–g. Fast decomposition was already
observed after addition of the first portion of borohydride. The results are summarized in Table 1. All
attempts to suppress decomposition by variations of reaction conditions (temperature, ratio of reagents,
solvent, reaction time, etc.) failed. To overcome this problem catalytic hydrogenation on palladium at
atmospheric pressure was tested. The reaction time at atmospheric pressure was quite long (10–48 h)
and satisfactory results were achieved in case of phenyl and unsubstituted furyl derivatives. The results
showed that the reaction of substituted furan-containing olefins did not proceed cleanly, and the
formation of side products, impurities and decomposition was noticed. In the case of 5-nitrofuran
derivative 1e only decomposition was observed, probably caused by instability of the partially reduced
nitrofuran function. Sulphur containing compounds 3f,3g were not tested due to anticipated catalyst
poisoning.
Scheme 1. Standard synthesis of 3-phenyl-2-cyanopropenenitrile, 3-(thiophen-2-yl)-2-
cyanopropenenitrile and 3-(furan-2-yl)-2-cyanopropenenitriles 1a–g.
CN
CN
piperidinecat
EtOH
O
X
X
Y
Y
1a-g
Y = (CH=CH), S, O
X = H, Br, NO2, C6H5S, CH3C6H4SO2
Table 1. Reaction of 3-phenyl, 3-(thiophen-2-yl) and 3-(5-substituted furan-2-yl)-2-
cyanopropenenitriles 1a–g with 2-phenylbenzimidazoline (2, PBI) generated in situ and
with NaBH4.
Entry
1a
Substrate
Y = (CH=CH), X = H
Y = S, X = H
Product
Yield a (%)
83 b (85) c
78 b (69) c
72 b (61) c
80 b (-) c,d
62 b (-) c,e
79 b (-) c,e
85 b (-) a,e
Time (h)
12 b (2) c
8 b (2) c
8 b (2) c
8 b (1) c
6 b (1) c
12 b (1) c
8 b (1) c
3a
3b
3c
3d
3e
3f
1b
1c
Y = O, X = H
1d
Y = O, X = Br
1e
Y = O, X = NO2
Y = O, X = C6H5S
1f
1g
Y = O, X = CH3C6H4SO2
b
3g
a
c
isolated yield; results obtained with PBI in ethanol; results obtained with NaBH4 in methanol;
d partial decomposition; e decomposition.
From these tests it was evident that we must look for milder and more selective reducing agent.
Herein, we decided to explore 2-phenylbenzimidazoline (2 PBI) as an organic hydride compound to
test its abilities in reducing electron-deficient olefins with electron-withdrawing substituents (CN

Molecules 2013, 18
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groups) of the furan series. 2-Phenylbenzimidazoline (2 PBI) is unstable in the air and easily oxidized
to aromatic
2-phenylbenzimidazole [24]. Therefore, 2-phenylbenzimidazoline is formed in situ from the ordinary
chemicals (i.e., 1,2-diaminobenzene and benzaldehyde) and is expected to be useful as a convenient,
mild and selective agent for the reduction of carbon-carbon double bonds in α,β-unsaturated dinitriles
1a–g. After the reaction of an equimolar amount of 1,2-diaminobenzene and benzaldehyde in ethanol
at room temperature in the presence of the same amount of 3-(5-nitrofuran-2-yl)-2-cyanopropenenitrile
(1e), 2-[(5-nitrofuran-2-yl)methyl]propanedinitrile (3e) was obtained in 62% yield. Although a nitro
group was inert towards 2-phenylbenzimidazoline, olefinic double bonds conjugated with nitrile
groups were reduced efficiently. For optimizing the conditions, several tests with various solvents
(MeOH, THF, CH3CN, DMF) were performed. When methanol or tetrahydrofuran were used as a
solvent the reaction proceeded smoothly, but the reaction time was longer, probably due to the lower
solubility of the starting material 3-(5-nitrofuran-2-yl)-2-cyano-propenenitrile (1e). Acetonitrile and
even more dimethylformamide as reaction solvent catalyzed slow formation of side products.
Consequently, ethanol remains as an optimal solvent. When attempts were made to improve the yields
and remove the traces of starting α,β-unsaturated dinitrile from the reaction mixtures by increasing the
amount of the reagent to 1.2 equivalents, the results showed a disappearance of starting material but
the product was a complex mixture. The residues of reducing agent remain in the product. Therefore,
all of the experiments were performed with equimolar amounts. In all cases, carbon-carbon double
bonds of the 3-(5-substituted furan-2-yl)-2-cyanopropenenitriles were selectively reduced in good
yields to give the corresponding 2-[(5-substituted furan-2-yl)methyl]propanedinitriles, while
conjugated cyano groups were unaffected, according to Scheme 2.
Scheme 2. Chemoselective reduction of conjugated double bonds with nitrile groups and
furan rings accomplished by using 2-phenylbenzimidazoline.
H
N
H
N
H
2 PBI
CN
CN
CN
CN
X
X
Y
Y
1a-g
3a-g
H
N
NH2
NH2
OHC
N
Y = (CH=CH), S, O
X = H, Br, NO2, C6H5S, CH3C6H4SO2
2-Benzylpropanedinitrile (3a), 2-[(thiophen-2-yl)methyl]propanedinitrile (3b) and 2-[(furan-2-
yl)methyl]propanedinitrile (3c) were also synthesized by reduction with 2-phenylbenzimidazoline

Molecules 2013, 18
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(2 PBI) formed in situ as well as by NaBH4 reduction. All of the results are summarized in Table 1. In
this reaction system, the isolation of 2-benzimidazoline (2 PBI) cannot be achieved, but it is smoothly
converted under the reaction conditions to 2-benzimidazole in a practically quantitative yield. After the
reaction when ethanol is evaporated, the 2-benzimidazole formed is removed from the reaction mixture
by simple filtration of the methylene chloride solution, where this compound is not soluble. The
remaining filtrate contains products 3a–g in sufficient (>95%) purity according to HPLC analysis. For
analytical purposes the final products were purified by column chromatography and/or
recrystallization.
3. Experimental
3.1. General
All chemicals were reagent grade and were purchased from Sigma-Aldrich (St. Louis, MO, USA)
and Acros Organics (Geel, Belgium). TLC analysis was performed on precoated 60 F254 plates (Merck,
Darmstadt, Germany). Compounds were visualized by UV light (254 nm) and evaluated in iodine vapour.
HPLC monitoring analyses were performed on an Agilent 1200 series HPLC system equipped with a
diode array detection (DAD) system, a quarternary model pump and an automatic injector (Agilent
Technologies, Santa Clara, CA, USA). ChemStation Chromatography Software was used for data
acquisition. Acetonitrile (HPLC grade, Sigma-Aldrich, 50.0%) and H2O (HPLC grade, Sigma-Aldrich,
50.0%) were used as the mobile phase. A Gemini-NX 100 (Phenomenex, Torrance, CA, USA), C18 3 μm,
2.0 × 100 mm chromatographic column was used with a total flow of 0.2 mL/min, an injection volume
of 5 μL and a column temperature of 35 °C. A detection wavelength of 210 nm was chosen. The
melting points were determined on a Boetius PHMK 05 (VEB Kombinat Nagema, Radebeul,
1
13
Germany) and are uncorrected. All H and C-NMR spectra were recorded in DMSO-d6 solutions at
ambient temperature on a Bruker Avance III 400 MHz spectrometer (Karlsruhe, Bruker, Germany,
400 MHz for 1H, 100 MHz for 13C). Chemical shifts are reported in ppm (). Proton chemical shifts in
DMSO-d6 are related to the middle of the solvent multiplet (δ = 2.50). 13C-NMR spectra were
measured using APT pulse sequences. Carbon chemical shifts are referenced to the middle of the
solvent multiplet (δ = 39.5 in DMSO-d6). Mass spectra were measured using a LTQ Orbitrap Hybrid
Mass Spectrometer (Thermo Electron Corporation, Waltham, MA, USA) with direct injection into an
APCI source (400 °C) in the positive mode.
3.2. Synthesis
3.2.1. Procedure for the Synthesis of 3-(Phenyl)-2-cyanopropenenitrile (1a) [29]
To the stirred solution of propanedinitrile (0.66 g, 10 mmol) in absolute ethanol (20 mL) under
argon was added benzaldehyde (1.06 g, 10 mmol) followed by 2–3 drops of piperidine. The reaction
was refluxed for 2–3 h. The precipitate was formed on cooling the reaction mixture to room
temperature. The crude product was filtered and recrystallized from ethanol to yield 3-phenyl-2-
cyanopropenenitrile (1a) in 75% yield.

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3.2.2. General Procedure for the Synthesis of 3-(Thiophen-2-yl) and 3-(5-Substituted Furan-2-yl)-2-
cyanopropenenitriles 1b–g [28,29]
To the stirred solution of propanedinitrile (0.66 g, 10 mmol) in absolute ethanol (20 mL) under
argon was added 2-thenaldehyde or 5-substituted furan-2-carbaldehyde (10 mmol) followed by 2–3 drops
of piperidine. The reaction was stirred for 2–3 h at room temperature. The precipitate was formed
during the reaction. The crude product was filtered, washed with cold ethanol and recrystallized from
ethanol to yield cyanopropenenitriles 1b–g in 56%–87% yields.
3.2.3. Procedure for the Synthesis of 2-Benzylpropanedinitrile with NaBH4
3-Phenyl-2-cyanopropenenitrile (1a, 1.54 g, 10 mmol) was dissolved in methanol (50.0 mL) at
room temperature. Then 757 mg (20 mmol) of NaBH4 were added in portions. The reaction mixture
was stirred at the same temperature for 2 hours, then cooled in ice-bath and 100 ml of water were
added. Precipitated crude product was filtrated and recrystallized from ethanol to yield 2-
benzylpropanedinitrile in 85% yield.
3.2.4. General Procedure for the Synthesis of Phenyl-, Thiofen-2-yl and 5-Substituted
Furan-2-ylmethylpropanedinitriles 3a–g with 2-Phenylbenzimidazoline (2 PBI)
Aryl or heteroaryl 2-cyanopropenenitrile (1a–g, 10 mmol) was dissolved in 96% ethanol (100 mL)
under argon. To a stirred mixture was added freshly distilled benzaldehyde (1.06 g, 10 mmol) at room
temperature, followed by 1,2-diaminobenzene (1.08 g, 10 mmol). Reaction mixture was stirred at the
same temperature and monitored by TLC. After completion of the reaction, ethanol was removed
under reduced pressure and the residue was triturated with methylene chloride (30 mL). Precipitated
2-phenylbenzimidazole was filtrated off and washed with methylene chloride (2 × 10 mL). Methylene
chloride was removed from combined filtrates under reduced pressure to yield arylmethyl or
heteroarylmethylpropanedinitriles 3a–g. The crude products were sufficiently pure for further
synthesis. For analytical purposes the products were purified by column chromatography and/or
recrystallization (Table 1).
2-Benzylpropanedinitrile (3a). Yield 83%; M.p. 90–91 °C (M.p. 88–91 °C [37]); 1H-NMR (DMSO-d6),
13
δ: 7.35–7.48 (m, 5H), 4.35 (t, J = 7.0 Hz, 1H), 3.37(d, J = 7.0 Hz, 2H); C-NMR (DMSO-d6), δ:
135.35, 129.94, 129.32, 128.35, 114.57 (2C), 35.01, 24.92.
2-[(Thiophen-2-yl)methyl]propanedinitrile (3b). Yield 78%; Colourless oil (M.p. 46.5–47 °C [36]);
1H-NMR (DMSO-d6), δ: 7.48 (d, J = 5.1 Hz, 1H), 7.23 (d, J = 3.2 Hz, 1H), 7.01 (dd, J = 5.1, 3.2 Hz,
13
1H), 4.25 (t, J = 6.6 Hz, 1H), 3.56 (d, J = 6.6 Hz, 2H); C-NMR (DMSO-d6), δ: 134.55, 129.82,
128.15, 127.16, 111.99 (2C), 31.53, 25.95.
1
2-[(Furan-2-yl)methyl]propanedinitrile (3c) [38]. Yield 72%; Yellowish oil; H-NMR (DMSO-d6), δ:
7.56 (dd, J = 1.8, 0.8 Hz, 1H), 6.40–6,35 (m, 2H), 4.64 (t, J = 7.0 Hz, 1H), 3.42 (d, J = 7.0 Hz, 2H);
13C-NMR (DMSO-d6), δ: 147.02, 143.67, 112.89 (2C), 110.12, 109.21, 29.80, 23.01.

Molecules 2013, 18
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1
2-[(5-Bromofuran-2-yl)methyl]propanedinitrile (3d) [39]. Yield 80%; Colourless oil; H-NMR
(DMSO-d6), δ: 6.58 (d, J = 3.3 Hz, 1H), 6.48 (dt, J = 3.3, 0.73 Hz, 1H), 5.15 (t, J = 6.2 Hz, 2 H), 3.48
13
(d, J = 6.2 Hz, 1 H); C-NMR (DMSO-d6), δ: 150.93, 121.27, 113.57 (2C), 112.78, 112.23, 27.92,
22.42; HR-MS: for C8H6BrN2O [M+H]+ calculated 224,9664 m/z, found 224,9683 m/z.
1
2-[(5-Nitrofuran-2-yl)methyl]propanedinitrile (3e). Yield 62%; Brownish oil; H-NMR (DMSO-d6),
δ: 7.41 (d, J = 3.3 Hz, 1H), 6.52 (d, J = 3.3 Hz, 1H), 4.92 (t, J = 6.5 Hz, 2H), 3.55 (d, J = 6.5 Hz, 1H);
13C-NMR (DMSO-d6), δ: 158.62, 150.74, 114.25, 112.87 (2C), 109.39, 27.85, 22.68,; HR-MS: for
C8H6N3O3 [M+H]+ calculated 192.0404 m/z, found 192.0438 m/z.
1
2-{[(5-(Phenylsulfanyl)furan-2-yl]methyl}propanedinitrile (3f). Yield 79%; Yellowish oil; H-NMR
(DMSO-d6), δ: 7.58–7.39 (m, 5H), 6.51 (d, J = 3.3 Hz, 1H), 6.44 (d, J = 3.3 Hz, 1H), 5.01 (t, J = 6.5 Hz,
2H), 3.52 (d, J = 6.5 Hz, 1H);13C-NMR (DMSO-d6), δ: 154.27, 142.15, 135.61, 131.16, 129.56,
125.58, 113.86 (2C), 112.91, 112.35, 27.21, 21.91; HR-MS: for C14H11N2OS [M+H]+ calculated
255.0587 m/z, found 255.0559 m/z.
2-({5-[(4-Methylphenyl)sulfonyl]furan-2-yl}methyl)propanedinitrile (3g). Yield 85%; M.p. 65–65 °C;
1H-NMR (DMSO-d6), δ: 7.74 (d, J = 8.0 Hz, 2H), 7.37 (d, J = 8.0 Hz, 2H), 6.56 (d, J = 3.4 Hz, 1H),
13
6.12 (d, J = 3.4 Hz, 1H), 4.89 (t, J = 6.6 Hz, 2H), 3.63 (d, J = 6.6 Hz, 1H), 2.32 (s, 3H); C-NMR
(DMSO-d6), δ: 155.21, 148.38, 145.95, 138.22, 130.14, 129.21, 112.33 (2C), 110.82, 107.19, 27.43,
22.19, 21.30; HR-MS: for C15H13N2O3S [M+H]+ calculated 301.0641 m/z, found 301.0657 m/z.
4. Conclusions
In summary, we have demonstrated that the reductions of -unsaturated dinitriles possessing
substituted furan rings could be achieved in high yields and chemoselectivity with 2-phenyl-
benzimidazoline (2, PBI) formed in situ. The easy work-up and separation of products make this
reinvented reagent a promising alternative reducing agent in organic synthesis. The reduction of furan
compounds 1a–g to 3a–g using PBI in ethanol was compatible with various substitution patterns and,
in the limited cases examined, with other functional groups (Table 1). A particular advantage of this
method over borohydride reduction and catalytic hydrogenation was the regioselective reduction of a
conjugated double bond in the presence of groups sensitive to reduction conditions or deactivating the
mostly used transition metals like palladium. The principal side reactions were not observed.
Acknowledgements
This study was supported by the IGA VFU Brno 51/2011/FaF and IGA VFU Brno 63/2011/FaF and
by institutional support RVO:68081715 from the Academy of Sciences of the Czech Republic.
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