Issue 11, 1973

α→β Rearrangements of naphthyl ketones under Friedel–Crafts acylation conditions

Abstract

The intramolecular acylation of the acid (I) by polyphosphoric acid (PPA) affords the kinetically controlled α-naphthyl ketone (II) and/or the thermodynamically controlled β-naphthyl ketone (III); (II) rearranges quantitatively to (III) with PPA at 120°.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1973, 362-363

α→β Rearrangements of naphthyl ketones under Friedel–Crafts acylation conditions

I. Agranat and D. Avnir, J. Chem. Soc., Chem. Commun., 1973, 362 DOI: 10.1039/C39730000362

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