The Reaction of α-Methylstyrene Analogs and Related Compounds With Sodium Perborate in Acetic Acid

John T. Gupton Department of Chemistry, University of Central Florida Orlando, Florida, 32816

Steven J. Duranceau Department of Chemistry, University of Central Florida Orlando, Florida, 32816

John F. Miller Department of Chemistry, University of Central Florida Orlando, Florida, 32816

Michael L. Kosiba Department of Chemistry, University of Central Florida Orlando, Florida, 32816

Abstract

A series of α-substituted styrene analogs have been reacted with sodium perborate in acetic acid to produce l-acetoxy-2-aryl-2-propanol analogs in good yield. The reaction constitutes a mild and convenient method for the oxidation of styrene type double bonds.

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The Reaction of α-Methylstyrene Analogs and Related Compounds With Sodium Perborate in Acetic Acid

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The Reaction of α-Methylstyrene Analogs and Related Compounds With Sodium Perborate in Acetic Acid

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