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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 41, 2011 - Issue 19
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Original Articles

Solvent-Free C-Benzoylation and N-Benzoylation Reactions Using Microwave Heating

, &
Pages 2888-2898 | Received 11 Jan 2010, Published online: 29 Jun 2011
 

Abstract

An ecofriendly and efficient microwave-irradiated solvent-free benzoylation method was developed. The procedure for C-benzoylation used 50 mol% AlCl3 as a Lewis acid catalyst at 130 °C and was completed in 10 min. The isolated yield was between 71% and 100%. N-benzoylation was conducted in a catalyst-free environment at 130 °C in 10 min. The isolated yield was between 80% and 100%.

ACKNOWLEDGMENT

Financial support from U.S. Department of Education Title III grant to Tennessee State University is acknowledged.

Notes

a All reactions were run at least two times. The products were purified by silica-gel chromatography using hexane/ethyl acetate (50/1) as the eluent.

a All reactions were run at least two times. The products were purified by silica-gel chromatography using hexane/ethyl acetate (5/1) as the eluent.

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