Journal of the Serbian Chemical Society (Jan 2001)

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

  • BOGDAN COMANITA,
  • IRINA POPOVICI,
  • EUGENIA COMANITA,
  • GHEORGHE ROMAN

Journal volume & issue
Vol. 66, no. 1
pp. 9 – 16

Abstract

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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.

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