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Synthesis and reactivity of some mannich bases. VIII. Studies on several mannich bases derived from ortho-hidroxyacetophenones and their conversion into oximino derivatives
- Source :
- Journal of the Serbian Chemical Society, Vol 66, Iss 1, Pp 9-16 (2001)
- Publication Year :
- 2001
- Publisher :
- Serbian Chemical Society, 2001.
-
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.
Details
- Language :
- English
- ISSN :
- 03525139 and 18207421
- Volume :
- 66
- Issue :
- 1
- Database :
- Directory of Open Access Journals
- Journal :
- Journal of the Serbian Chemical Society
- Publication Type :
- Academic Journal
- Accession number :
- edsdoj.01be9ff9fa4542a6bf2a2e8a58d8d1c8
- Document Type :
- article
- Full Text :
- https://doi.org/10.2298/JSC0101009C