Issue 10, 1998

Alumina in Methanesulfonic Acid (AMA) as a New Efficient Reagent for Direct Acylation of Phenol Derivatives and Fries Rearrangement. A Convenient Synthesis of o-Hydroxyarylketones

Abstract

Alumina in methanesulfonic acid is used to prepare o-hydroxyarylketones, by acylation of phenol and naphthol derivatives with carboxylic acids and Fries rearrangement of phenolic esters.

Article information

Article type
Paper

J. Chem. Res. (S), 1998, 628-629

Alumina in Methanesulfonic Acid (AMA) as a New Efficient Reagent for Direct Acylation of Phenol Derivatives and Fries Rearrangement. A Convenient Synthesis of o-Hydroxyarylketones

H. Sharghi and B. Kaboudin, J. Chem. Res. (S), 1998, 628 DOI: 10.1039/A800158H

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