Issue 0, 1968

Structural effects in reactions of organophosphorus compounds. I. Reactions of phosphorus oxychloride with hindered phenols

Abstract

2,6-Dialkyl-phenols exhibit little steric hindrance on reaction with phosphoryl chloride unless the alkyl substituent is bulky (i.e. t-butyl). Where bulky substituents are present reaction with phosphoryl chloride occurs only in the presence of Friedel–Crafts type catalysts after either a dealkylation or a rearrangement of the ortho-placed alkyl groups, followed by O-phosphorylation, has occurred.

Article information

Article type
Paper

J. Chem. Soc. C, 1968, 815-818

Structural effects in reactions of organophosphorus compounds. I. Reactions of phosphorus oxychloride with hindered phenols

G. M. Kosolapoff, C. K. Arpke, R. W. Lamb and H. Reich, J. Chem. Soc. C, 1968, 815 DOI: 10.1039/J39680000815

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