Synthesis and reactivity of some mannich bases. VIII. Studies on several mannich bases derived from ortho-hidroxyacetophenones and their conversion into oximino derivatives-Reference-Cited by-同舟云学术

Synthesis and reactivity of some mannich bases. VIII. Studies on several mannich bases derived from ortho-hidroxyacetophenones and their conversion into oximino derivatives

Published:2001 Issue:1 Volume:66 Page:9-16
ISSN:0352-5139
Container-title:Journal of the Serbian Chemical Society
language:en
Short-container-title:JSCS

Author:

Comanita Eugenia¹,Roman Gheorghe²,Popovici Irina³,Comanita Bogdan⁴

Affiliation:

1. "Gh. Asachi" Technical University, Department of Organic Chemistry, Romania

2. "Transilvania" University, Chemistry Department, Romania

3. "Gr. T. Popa" University of Medicine and Pharmacy, Romania

4. National Research Council of Canada, Institute for Chemical Process and Environmental Technology, Ottawa, Canada

Abstract

The synthesis of several Mannich bases resulting from the reaction of 2-hydroxy-4-methylacetophenone with paraformaldehyde and secondary amines is reported. Another series of products was obtained from N,N-dimethyl substituted Mannich bases by replacing the amino group with pyrrolidine. Most of the Mannich bases were transformed into oximes by treatment with hydroxylamine hydrochloride in 10% NaOH.

Publisher

National Library of Serbia

Subject

General Chemistry

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