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Article << Previous     |         Contents Vol 32(8)

Formation of ortho Diol Diacetates in the Acid-Catalysed Rearrangement of 4-Aryl-4-hydroxycyclohexa-2,5-dienones. A Structural Reassignment

DM Gash and PD Woodgate

Australian Journal of Chemistry 32(8) 1863 - 1867
Published: 1979

Abstract

Treatment of the p-quinols 2,6-di-t-butyl-4-hydroxy-4-phenylnaphthalen-1(4H)-one, 2,6-di-t-butyl-4-hydroxy-4-phenylcyclohexa-2,5-dienone and 2,6-di-t-butyl-4-hydroxy-4-(4'-methoxyphenyl)cyclohexa-2,5-dienone with acetic anhydride and sulfuric acid affords, as the major product, an aromatic ortho diol diacetate.



Full text doi:10.1071/CH9791863

© CSIRO 1979

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