Chem. J. Chinese Universities ›› 1990, Vol. 11 ›› Issue (9): 958.

• Articles • Previous Articles     Next Articles

A New Method foir the Synthesis of 5(4H)-Oxazolones from N-Acyl-a-Amiho Acids

Huang Huamin, Zhang Jianing, Wang Jingyang   

  1. Department of Chemistry, Jilin University, Changchun
  • Received:1989-04-17 Online:1990-09-24 Published:1990-09-24

Abstract: In K2CO3-CH3COCH3-H2O system, N-acyl-a-amino acids (Ⅰa-j) were prepared by the reaction of amino acids with N-acyl thiazolidines-2-thiones and the yields were 76%~95%. The synthesis of saturated 5(4H)-oxazolones(Ⅱa-h) from Iunder mild reaction conditions in yields of 43%~84% by the use of cyanuric chloride as a condensing reagent in the presence of triethylamine was reported. Unsaturated 5(4H)-oxazolones (Ⅲa-j) were obtained from Iin the yields of 43%~93% by the aldol reaction in which Fe2SO4)3 was used as a catalyst.

Key words: N-acyl-a-amino acid, Cyanuric chloride, Saturated 5(4H)-oxazolone, Unsaturated 5(4H)-oxazolone

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