Issue 0, 1967

Oxidation of alkoxyphenols. Part IX. A dipheno-2,2′-quinone from 2,2′-dihydroxy-5,5′-dimethoxy-4,4′-di-t-butylbiphenyl

Abstract

Oxidation by alkaline ferricyanide converts 2,2′-dihydroxy-5,5′-dimethoxy-4,4′-di-t-butylbiphenyl into an unstable dipheno-2,2′-quinone which decomposes in solution to a dibenzofuranquinone and a hydroxyphenyl-quinone. The latter is the only product on oxidation by ferric chloride. Oxidation by ceric sulphate or lead tetra-acetate results in demethylation and gives diquinone.

Article information

Article type
Paper

J. Chem. Soc. C, 1967, 723-725

Oxidation of alkoxyphenols. Part IX. A dipheno-2,2′-quinone from 2,2′-dihydroxy-5,5′-dimethoxy-4,4′-di-t-butylbiphenyl

F. R. Hewgill and D. G. Hewitt, J. Chem. Soc. C, 1967, 723 DOI: 10.1039/J39670000723

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