2009Synthetic CommunicationsRequires access

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

Gangadhar A. Meshram, Vishvanath D. Patil

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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.

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What this paper is about

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.

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Available 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.

Key concepts: Chemistry, Anhydrous, Acetic anhydride, Phenols, Organic chemistry, Solvent, Acetylation, Catalysis

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