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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

Polystyrene-Supported, Al(OTf)3-Catalyzed Chemoselective Synthesis of Acylals from Aldehydes

Pages 277-284 | Received 12 Aug 2009, Published online: 15 Dec 2010
 

Abstract

Cross-linked polystyrene-supported aluminium triflate [Ps-Al(OTf)3] has been shown to be a mild, efficient, and chemoselective heterogeneous Lewis acid catalyst for acetylation of aldehydes with acetic anhydride. The catalyst can be recovered simply and reused efficiently at least five times without any noticeable loss of catalytic activity.

ACKNOWLEDGMENT

The author thanks the Research Council of Shahrekord University for partial support of this work.

Notes

a The molar ratio of the aldehyde/Ac2O/cat. is 1:1.5:0.1 except for entries 1i and 3, in which the molar ratio is 1:2.5:0.12.

b Yields refer to pure isolated products, and all acylals prepared are known compounds and were characterized by comparison of their physical and spectral data with those of authentic samples.

a The molar ratio of substrate 1 to substrate 2 to Ac2O is 1:1:1.2 for entries 1 and 2 and 1:1:1 for entries 3 and 4.

b All reactions were carried out in CH2Cl2 at room temperature in the presence of 1 Ps-Al(OTf)3 (0.1 mmol), 2 Al(OTf)3 (0.2 mmol), or 3 AlCl3 (0.28 mmol).

c GC yield.

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