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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 39, 2009 - Issue 14
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Original Articles

Simple and Efficient Method for Acetylation of Alcohols, Phenols, Amines, and Thiols Using Anhydrous NiCl2 Under Solvent-Free Conditions

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Pages 2516-2528 | Received 11 Oct 2008, Published online: 16 Jun 2009
 

Abstract

Solvent-free acetylation of alcohols, phenols, amines, and thiols with acetic anhydride (Ac2O) in the presence of 0.1 mol% (13 mg) anhydrous NiCl2, an inexpensive and easily available catalyst. Excellent yields, short reaction time, and mild reaction conditions are important features of this method.

ACKNOWLEDGMENT

The authors acknowledge the partial support of this work by Prof. B. P. Bandgar, Vice chancellor, University of Solapur, India.

Notes

a Isolated yield of the corresponding acetylated product.

a The substrate was treated with 1 equiv. of the anhydride in the presence of 0.1 mol% (13 mg) of catalyst under solvent-free conditions at room temperature.

b Isolated yield of the corresponding acetylated product.

a Yields refer to pure products. All products were characterized by comparison of their IR spectra, 1H NMR spectra, and elemental analysis with those of authentic samples.

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