Document Type

Article

Keywords

Acetylated-2-amino-5-halophenols, 2-Acetamido-5-haloanisoles, 6-Halo-2-methylbenzoxazoles, 6-Halobenzoxazolones, 6-Halotriacetylaminophenols, 1H-NMR spectra, Fungicidal activity

Disciplines

Biochemistry

Abstract

The halogenation of derivatives of 2-aminophenol with N-chloro- and N-bromosuccinimides at ambient temperatures in acetic acid was studied. With the necessary compounds available, a reexamination of the thermolytic rearrangement of 2-halophenyl azides to 2-aminophenols and other products was undertaken. It is certain that the rearrangement of 4-halophenyl azides to 2-aminophenols occurs but the products identified in this study differ significantly from those reported previously by Suschitzky et al. (1963, 1966)

Article Number

1081

Publication Date

1993

Comments

Monatshefte für Chemie 124:367-379. http://0-dx.doi.org.library.simmons.edu/10.1007/BF00814133

Included in

Biochemistry Commons

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