Tandem bis-aldol reaction of ketones: A facile one-pot synthesis of 1,3-dioxanes in aqueous medium

Article abstract of DOI:10.1021/jo701337j

(Chemical Equation Presented) A novel tandem bis-aldol reaction of ketone with paraformaldehyde catalyzed by polystyrenesulfonic acid in aqueous medium delivers 1,3-dioxanes in high yield. This one-pot, operationally simple microwave-assisted synthetic pr

Full text of DOI:10.1021/jo701337j

alcohol depending on the reaction conditions.7 In fact, several
groups have taken advantage of this transformation as an
efficient approach to natural product targets.8
Tandem Bis-aldol Reaction of Ketones: A Facile
One-Pot Synthesis of 1,3-Dioxanes in Aqueous
Medium
While dioxanes have great potential as a drug candidate, the
synthetic protocol of this important molecule has been largely
untapped. In view of our ongoing research effort devoted to
the development of greener synthetic pathways for a range of
bioactive molecules,9 herein, we report a novel tandem bis-aldol
reaction of ketones with paraformaldehyde catalyzed by polymer-
supported polystyrenesulfonic acid (PSSA) under microwave
(MW) irradiation in aqueous media to yield 1,3-dioxanes
(Scheme 1).
Vivek Polshettiwar and Rajender S. Varma*
Sustainable Technology DiVision, National Risk Management
Research Laboratory, U. S. EnVironmental Protection Agency,
MS 443, Cincinnati, Ohio 45268
Varma.rajender@epa.goV
ReceiVed June 21, 2007
SCHEME 1. Bis-aldol Reaction of Flavanone in Water
We initially investigated the reaction of acetophenone with
paraformaldehyde to establish the feasibility of our strategy to
1,3-dioxane systems and to optimize the reaction conditions
(Table 1).
TABLE 1. Optimization of Reaction Conditions with Use of MW
Irradiation
temp
(°C)
reaction
time (min)
yield
(%)
A novel tandem bis-aldol reaction of ketone with paraform-
aldehyde catalyzed by polystyrenesulfonic acid in aqueous
medium delivers 1,3-dioxanes in high yield. This one-pot,
operationally simple microwave-assisted synthetic protocol
proceeds efficiently in water in the absence of organic
solvent, with excellent yield.
entry
catalyst
solvent
1
2
3
4
5
6
7
MeOH
MeOH
MeOH
100
120
120
120
120
120
sonication
60
45
45
45
45
30
24 h
NR
NR
NR
25
81
83
clay
Nafion
AcOH
TFA
PSSA
PSSA
water
water
NR
Dioxane rings are common structural motifs in numerous
bioactive molecules such as (+)-Dactylolide (a cytotoxic agent),1
derivatives of 2-substituted-1,3-dioxanes (antimuscarinic agents),2
and (+)-SCH 351448 (a novel activator of low-density lipo-
protein receptor promoters).3 A variety of biologically active
molecules have been identified from libraries of diverse, natural
product-like 1,3-dioxanes.4 Recently 1,3-dioxane derivatives
have been found to be effective modulators for multidrug
resistance.5 Over the years, there has been a plethora of elegant
methodologies developed independently for the synthesis of
these molecules. The acid-catalyzed condensation of olefins with
aldehyde known as Prins reaction is generally used for these
dioxane syntheses.6 The major product of this reaction consists
of tetrahydropyran, 1,3-dioxane, 1,3-glycol, or an unsaturated
First the reaction was conducted without any catalyst by using
MW and no reaction (NR) was observed. Then montmorillonite-
K10 (clay) and Nafion-H catalysts in methanol (MeOH) were
tested and in both these conditions, little dehydrated product
and no bis-aldol products were obtained. Acetic acid (AcOH)
did catalyze the reaction, but the yield was very poor. However,
trifluroacetic acid (TFA) and PSSA did efficiently catalyze this
reaction and afforded high yields of the desired product.
(7) (a) Fuson, R. C.; Ross W. E.; McKeever, C. H. J. Am. Chem. Soc.
1938, 60, 2935-2936. (b) Lumma W. C.; Ma, O. H. J. Org. Chem. 1970,
35, 2391-2393. (c) Jasti R.; Rychnovsky, S. D. J. Am. Chem. Soc. 2006,
128, 13640-13648. (d) Barluenga, J.; Dieguez, A.; Fernandez, A.;
Rodriguez F.; Fananas, F. J. Angew. Chem., Int. Ed. 2006, 45, 2091-2093.
(e) Cho, Y. S.; Karupaiyan, K.; Kang, H. J.; Pae, A. N.; Cha, J. H.; Koh,
H. Y.; Chang, M. H. Chem. Commun. 2003, 2346-2347.
(8) (a) Adams, D. R.; Bhaynagar, S. D. Synthesis 1977, 661-672. (b)
Snider, B. B. The Prins and Carbonyl Ene Reactions. In ComprehensiVe
Organic Synthesis; Trost, B. M., Ed.; Pergamon Press: Oxford, UK, 1991;
Vol. 2, pp 527-561.
(9) (a) Polshettiwar, V.; Varma, R. S. Tetrahedron Lett. 2007, 48, 5649-
5652. (b) Ju, Y.; Kumar, D.; Varma, R. S. J. Org. Chem. 2006, 71, 6697-
6700. (c) Ju, Y.; Varma, R. S. J. Org. Chem. 2006, 71, 135-141. (d) Ju,
Y.; Varma, R. S. Org. Lett. 2005, 7, 2409-2411. (e) Wei, W.; Keh, C. C.
K.; Li, C.-J.; Varma, R. S. Clean Technol. EnViron. Policy 2005, 7, 62-
69. (f) Kumar, D.; Chandra Sekhar, K. V. G.; Dhillon, H.; Rao, V. S.;
Varma, R. S. Green Chem. 2004, 6, 156-157. (g) Yang, X. -F.; Wang,
M.; Varma, R. S.; Li, C.-J. Org. Lett. 2003, 5, 657-660.
(1) Aubele, D. L.; Wan, S.; Floreancig, P. E. Angew. Chem., Int. Ed.
2005, 44, 3485-3488.
(2) Marucci, G.; Piero, A.; Brasili, L.; Buccioni, M.; Giardina`, D.; Gulini,
U.; Piergentili, A.; Sagratini, G. Med. Chem. Res. 2005, 14, 274-296.
(3) Chan, K.; Ling Y. H.; Loh, T. Chem. Commun. 2007, 939-941.
(4) (a) Shang S.; Tan, D. S. Curr. Opin. Chem. Biol. 2005, 9, 248-258.
(b) Wong, J. C.; Sternson, S. M.; Louca, J. B.; Hong, R.; Schreiber, S. L.
Chem. Biol. 2004, 11, 1279-1291. (c) Pinilla, C.; Appel, J. R.; Borras E.;
Houghten, R. A. Nat. Med. 2003, 9, 118-122.
(5) Schmidt, M.; Ungvari, J.; Glode, J.; Dobner, B.; Langner, A. Bioorg.
Med. Chem. 2007, 15, 2283-2297.
(6) Yang, N. C.; Yang, D. H.; Ross, C. B. J. Am. Chem. Soc. 1959, 81,
133-136.
10.1021/jo701337j CCC: $37.00 © 2007 American Chemical Society
Published on Web 08/16/2007
7420
J. Org. Chem. 2007, 72, 7420-7422

TABLE 2. Tandem Bis-aldol Reaction of Ketones with
Paraformaldehyde Catalyzed by PSSA in Water
In view of the emerging MW chemistry interest in aqueous
reaction medium,10 and in keeping with our emphasis on
exploration of cleaner pathways,9 we tried to develop greener
reaction conditions and observed that PSSA efficiently catalyzed
this reaction in water. Thus, we have developed an aqueous
one-pot protocol for the tandem bis-aldol reaction of ketone
with paraformaldehyde. To further define the scope of this
reaction, a wide variety of ketones were evaluated for this
cyclization reaction and the results are summarized in Table 2.
Various ketones reacted efficiently with paraformaldehyde
to afford the desired 1,3-dioxanes in good yield (entries 1-7).
This approach establishes a convenient and flexible method to
attach functional arms to indanone and flavanone (entries 8 and
9) for further elaboration in synthetic design. The aliphatic
ketones, however, afforded low yields (entries 10-12), which
may be due to their unavoidable self-condensation. 1-Methyl-
2-pyrrolidinone (entry 11) gave no product indicating the
nonreactivity of amide carbonyl toward this reaction. The
reaction is completed under conventional heating in an oil bath
at the same temperature to afford comparable yields but requires
an extended period of time, 4-5 h.
It is noteworthy to mention that these reactions are working
well in an aqueous medium without using any phase-transfer
catalyst (PTC). This may be due to selective absorption of
microwaves by reactants, intermediates, and polar aqueous
medium,10 which accelerate the reaction even in the absence of
PTC. In most of the experiments, we observed that after
completion of reactions, the phase separation of the desired
product from the aqueous media occurs under hot condition,
which facilitates isolation of the crude product by simple
decantation instead of tedious extraction processes, thus reducing
the use of volatile organic solvents for extraction. As exemplified
by the reaction of flavanone with paraformaldehyde in PSSA/
water, a distinct phase separation was exhibited (as shown in
the graphical abstract).
The mechanism of the similar cyclization reaction has been
studied by Ross et al. in the synthesis of 1,3-dioxanes from
alkene and aldehyde,6 stereoaspects of which were then explored
by Portoghese et al.11 We postulate the following mechanism
for the PSSA-catalyzed tandem bis-aldol reaction of ketone with
paraformaldehyde in water (Scheme 2).
SCHEME 2. Mechanism of the Bis-aldol Reaction
The reaction involved the addition of a protonated formal-
dehyde (generated by microwave exposure of paraformaldehyde
with PSSA/water) molecule to ketone (enol) to form â-hydroxy
a GC yields (isolated yield). All compounds were characterized by MS,
1H NMR, and 13C NMR.
(10) (a) Dallinger, D.; Kappe, C. O. Chem. ReV. 2007, 107, 2563-2591.
(b) Iimura, S.; Manabe, K.; Kobayashi, S. Org. Biomol. Chem. 2003, 1,
2416-2418.
(11) Smissman, E. E.; Schnettler, R. A.; Portoghese, P. S. J. Org. Chem.
1965, 30, 797-801.
ketone I. This was followed by the addition of another
protonated formaldehyde molecule to I to yield diol II, that in
turn attacks the third formaldehyde molecule to give adduct III,
which after dehydration yields the final product 1,3-dioxane IV.
J. Org. Chem, Vol. 72, No. 19, 2007 7421

13C NMR (CDCl3) δ 198, 135, 133, 132, 130, 129, 128, 127, 126,
In conclusion, we have demonstrated a new and efficient
approach to attach 1,3-dioxane functional arms to ketones. This
reaction will be very useful in drug discovery for the synthesis
of bioactive molecules bearing a 1,3-dioxane moiety. Also the
use of polymer-supported commercially available, and inex-
pensive PSSA as a catalyst and water as a reaction medium are
additional eco-friendly attributes of this synthetic protocol.
124, 93, 69, 44; MS 242 (M+), 212, 170, 155 (b), 127, 101, 77.
1
Entry 4: H NMR (CDCl3) δ 7.9 (d, 2H), 7.6 (m, 3H), 5.1 (d,
1H), 4.7 (d, 1H), 4.2 (d, 2H), 3.9 (m, 3H); 13C NMR (CDCl3) δ
197, 138, 134, 130, 129, 93, 68, 43; MS 270 (M+), 240, 227, 211,
198, 183, 155, 132, 104, 76, 55.
1
Entry 5: H NMR (CDCl3) δ 7.9 (d, 2H), 7.6 (m, 3H), 5.1 (d,
1H), 4.7 (d, 1H), 4.3 (d, 2H), 4 (m, 3H); 13C NMR (CDCl3) δ 198,
139, 134, 131, 130, 94, 68, 44; MS 318 (M+), 288, 246, 231, 203,
132, 104, 76, 55.
Experimental Section
1
Entry 6: H NMR (CDCl3) δ 7.2-7.4 (m, 4H), 5 (d, 1H), 4.8
All starting ketones and paraformaldehyde were used as ob-
tained. TLC (silica gel; 20% EtOAc:hexane) and GC-MS was used
to monitor the reactions. The crude products were identified by
GC/MS qualitative analysis, using a GC system with a mass
selective detector. The identities were further confirmed by 1H and
13C NMR spectra that were recorded in chloroform-d (CDCl3)
with TMS as internal reference, using a 300 MHz NMR spectrom-
eter.
(d, 1H), 3.7-4.2 (m, 5H); 13C NMR (CDCl3) δ 201, 138, 133,
131, 129, 127, 93, 68, 43; MS 225 (M+), 196, 179, 167, 154, 139,
131, 111, 75, 55.
Entry 7: 1H NMR (CDCl3) δ 7.3-7.5 (m, 4H), 4.9 (d, 1H), 4.7
(d, 1H), 3.7-4.1 (m, 5H); 13C NMR (CDCl3) δ 202, 139, 132,
130, 128, 126, 94, 68, 44; MS 270 (M+), 242, 198, 183, 155, 132,
104, 76, 55.
1
Entry 8: H NMR (CDCl3) δ 7.5 (m, 3H), 5.2 (d, 1H), 4.8 (d,
Typical Experimental Procedure: The ketone (5 mmol) and
paraformaldehyde (20 mmol) were placed in a 10 mL crimp-sealed
thick-walled glass tube equipped with a pressure sensor and a
magnetic stirrer. The contents were dissolved in 20% PSSA solution
in water (five times the weight of ketone) and the reaction tube
was placed inside the cavity of a CEM Discover focused microwave
synthesis system, operated at 120 ( 5 °C (temperature monitored
by a built-in infrared sensor), power 40 to 140 W, and pressure
40-70 psi for 30 min (Table 2). After completion of the reaction,
the phase separation of the desired product from the aqueous media
occurs, facilitating the isolation of crude product by simple
decantation, which was subjected to column chromatography to
afford pure 1,3-dioxanes.
1H), 4 (d, 2H), 3.8 (d, 2H), 3.4 (s, 2H); 13C NMR (CDCl3) δ 201,
134, 131, 129, 126, 93, 72, 39; MS 282 (M+), 264, 236, 223, 196,
144, 115 (b), 89, 63.
1
Entry 9: H NMR (CDCl3) δ 7.8 (d, 1H), 7.5 (t, 1H), 7.3 (m,
5H), 7.1 (m, 2H), 6.1 (s, 1H), 5.1 (d, 1H), 4.7 (d, 1H), 4.4 (m,
2H), 3.8 (d, 2H); 13C NMR (CDCl3) δ 195, 160, 138, 136, 127,
126, 124, 121, 119, 93, 80, 70, 68; MS 296 (M+), 266, 250, 235,
207, 175, 145, 121 (b), 92, 77.
1
Entry 10: H NMR (CDCl3) δ 4.9 (d, 1H), 4.7 (d, 1H), 4.3 (d,
2H), 3.5 (d, 2H), 2.3 (s, 3H), 1 (s, 3H); 13C NMR (CDCl3) δ 210,
94, 72, 48, 26, 18; MS 144 (M+), 126, 114 (b), 101, 84, 69, 57.
Acknowledgment. Vivek Polshettiwar was supported, in
part, by the Postgraduate Research Program at the National Risk
Management Research Laboratory administered by the Oak
Ridge Institute for Science and Education through an interagency
agreement between the U.S. Department of Energy and the U.S.
1
Entry 1: H NMR (CDCl3) δ 8 (d, 2H), 7.5 (m, 3H), 5.1 (d,
1H), 4.7 (d, 1H), 4.3 (d, 2H), 4 (m, 3H); 13C NMR (CDCl3) δ 196,
135, 133, 128, 127, 93, 69, 43; MS 191 (M+), 162, 145, 133, 120,
105, 77, 51.
1
Entry 2: H NMR (CDCl3) δ 8.3 (d, 2H), 8.1 (d, 2H), 5.1 (d,
1H), 4.7 (d, 1H), 4.3 (d, 2H), 3.9 (m, 3H); 13C NMR (CDCl3) δ
198, 153, 140, 128, 124, 94, 68, 41; MS 236 (M+), 207, 178, 150,
132, 104, 76, 55.
Supporting Information Available: Experimental procedures,
and NMR and MS data of compounds (entries 1-10). This material
is available free of charge via the Internet at http://pubs.acs.org.
1
Entry 3: H NMR (CDCl3) δ 8.5 (s, 1H), 8 (m, 4H), 7.6 (m,
2H), 5.1 (d, 1H), 4.7 (d, 1H), 4.4 (d, 2H), 4 (d, 2H), 3.3 (s, 1H);
JO701337J
7422 J. Org. Chem., Vol. 72, No. 19, 2007