Chem. J. Chinese Universities ›› 1982, Vol. 3 ›› Issue (S1): 83.

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MANNICH REACTION WITH ARYLAMINE AS THE AMINECOMPONENT (Ⅱ)——SYNTHESIS OF β-ARYLAMINOKETONE USING ARYLAMINE HYDROCHLORIDE

Chen Guangxu, Xu Xiujuan, Liu Lijun   

  1. Department of Chemistry, Beijing Normal University, Beijing
  • Received:1982-03-09 Online:1982-12-31 Published:1982-12-31

Abstract:

Mannich reaction was carried out directly between arylatnine hydrochloride, 37% formaldehyde and alkylarylketone, methylalkylketone or cycloke-tone by the following method: To arylamine dissolved in ethyl alcohol, a solution of ethanolic-HCl was added. Without separating the arylamine hydrochloride which settled out readily, a mixture of 37% formaldehyde and appropriate ketone was added, and the mixture thus obtained was allowed to stand a few hours or over night at room temperature. β-Arylaminoketone hydrochloride which crystallized out during this period was separated and worked up. This is a new method for the direct synthesis of β-arylaminoketones through Mannich reaction. The yields were satisfactory.

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