Issue 19, 1973

Conversion of o-hydroxyaldehydes and ketones into o-hydroxyanilides by monochloramine

Abstract

Rearrangement of the sodium salts of salicylaldehyde, 2-hydroxyacetophenone, and o-vanillin by monochloramine yielded 2-formamidophenol (88%), 2-acetamidophenol (93%), and 2-formamido-6-methoxyphenol (75%), respectively.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1973, 716-717

Conversion of o-hydroxyaldehydes and ketones into o-hydroxyanilides by monochloramine

R. A. Crochet and P. Kovacic, J. Chem. Soc., Chem. Commun., 1973, 716 DOI: 10.1039/C39730000716

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