Chem. J. Chinese Universities ›› 2003, Vol. 24 ›› Issue (7): 1222.

• Preface • Previous Articles     Next Articles

Studies on the Condensation Reaction of α,α-Diacetyl Ketene Dithioacetals with Arylaldehydes

AI Lin1,2, LIU Qun1, LI Xiao-Fang1, WANG Mang1   

  1. 1. Faculty of Chemistry, Northeast Normal University, Changchun 130024, China;
    2. Department of Chemistry, Beijing Normal University, Beijing 100875, China
  • Received:2002-07-03 Online:2003-07-24 Published:2003-07-24

Abstract: The condensation reactions of α,α-diacetyl ketene dithioacetals with arylaldehydes catalyzed by sodium tert-butoxide were performed. These reactions were affected by the alkylthio groups. The deacylation-condensation products α-cinnamoyl ketene dibenzylthioacetals 4 were obtained by the reaction of α,α-diacetyl ketene dibenzylthioacetals 1 with arylaldehydes 3. α,α-Dicinnamoyl ketene cyclic dioacetals 5 was formed when the reaction was performed between α,α-diacetyl ketene cyclic dioacetals 4 and arylaldehydes 3.

Key words: α,α-Diacetyl ketene dithioacetals, Arylaldehydes, Condensation

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