Abstract
An efficient solid-phase benzoylation of phenols and alcohols was developed under microwave irradiation. A stoichiometric amount of benzoyl chloride was sufficient to carry out the reaction. This benzoylation features short reaction time, good yields, and easy workup procedures. Furthermore, the scope of the reaction was extended to prepare 3,5-dinitrobenzoyl derivatives of alcohols.
GRAPHICAL ABSTRACT
ACKNOWLEDGMENTS
The authors are thankful to Nandita Basu (Ghorai), director, and Santanu Tripathi, head of the Department of Clinical and Experimental Pharmacology, School of Tropical Medicine, Kolkata, for their cooperation. The authors are also thankful to Dr. Gautam Chattopadhyay, Ex-reader in Chemistry, Presidency College, Kolkata, for his insightful discussions.
SUPPLEMENTAL MATERIAL
Full experimental details, 1H and 13C NMR spectra, and additional references for this article can be accessed on the publisher’s website.