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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 41, 2010 - Issue 2
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Original Articles

Conjugate Polymer-Supported Acid Catalysts: An Efficient and Reusable Catalyst for the Synthesis of Geminal Diacetates (Acylals) Under Solvent-Free Conditions

, &
Pages 191-199 | Received 08 Oct 2009, Published online: 15 Dec 2010
 

Abstract

A comparative study on the catalytic activity of conducting polyaniline (PANI), polypyrrole (PPY), and poly-(3,4-ethylenedioxythiophene) (PEDOT) salts as solid acid catalysts for the synthesis of 1,1-diacetates (acylals) under solvent-free conditions has been presented. Use of the polypyrrole and poly-(3,4-ethylenedioxythiophene) salts as solid acid catalysts is reported for the first time. Preparation, recovery, and reusability of the catalysts were found to be good.

ACKNOWLEDGMENT

We gratefully acknowledge the financial support from the Research Council of Shahid Beheshti University.

Notes

a Reaction conditions: acetic anhydride (0.2 mL, 2 mmol), benzaldehyde (1 mmol), catalyst (1–5.4 mol%), 20 min, at rt.

b Isolated total yield.

c The yields of three subsequent runs using the same recovered catalyst.

d 30 °C for 5 h.

a Isolated yields.

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