Acylation Reactions of Phenylhydrazines. Preparation and Properties of New Diacylphenylhydrazines

Michael J. Hearn, Debra J. Magee, Randl Alhart, Marye Gleva, Susan Goldstein, Flona Levy, Colette Muenzen, Isabel Neuringer, Mary Racln, Judlth Rosenberg, Holly Silva, Paula Williams

Research output: Contribution to journalArticlepeer-review

6 Scopus citations

Abstract

Anhydride acylation reactions of a variety of substituted arylhydrazines under mild conditions led to controlled formation of the acid phenylhydrazides I (Table I). The procedures were tailored to the particular state of the starting arylhydrazine. Second-stage acylation of phenylhydrazides conveniently produced the N,N'-diacylphenylhydrazines II (Table II), In which the acyl groups were the same or nonidentical. β acylation of phenylhydrazine resulted In significant changes In the ultraviolet spectrum (Table III); the ultraviolet spectra thus provide useful data in the determination of the extent and site of acylation.

Original languageEnglish
Pages (from-to)129-131
Number of pages3
JournalJournal of Chemical and Engineering Data
Volume30
Issue number1
DOIs
StatePublished - Jan 1 1985
Externally publishedYes

Fingerprint Dive into the research topics of 'Acylation Reactions of Phenylhydrazines. Preparation and Properties of New Diacylphenylhydrazines'. Together they form a unique fingerprint.

Cite this