82415-85-8Relevant articles and documents
TRANSPOSITION DES OXIMES DE LA 2h-NAPHTOPYRANNONE-3 ET DE LA 2H-BENZOFURANNONE-3
Hardy, Jean-Claude,Venet, Marc
, p. 1255 - 1256 (1982)
Refluxing the oximes (2) of naphtopyran-3(2H)-one and (6) of 3(2H)-benzofuranone with alcoholic hydrogen chloride give the corresponding α-alkoxy-ketones 3, 4, 5 and α-chloroketone 7 respectively.This transformation appears to be related to the acid conversion of N-arylhydroxyamines to o. and p. substituted anilines (BAMBERGER rearrangement).