Ten N-substituted cinnamamides ( 3 a ~3 j ) were synthesized by chlorination of cinnamic acid with thionyl chloride in DMAc (4 mL) at 0 ℃for 20 min, followed by amidation with arylamines at 25 ℃for 3 h.The yield of 3a~3j were 85.8%~96.5%.The structures were confirmed by 1 H NMR, 13 C NMR, IR and EI-MS.The proposed mechanism for the promotion of DMAc for the reaction was suggested .%以肉桂酸为原料,N,N-二甲基乙酰胺( DMAc,4 mL)为促进剂,先与SOCl2于0℃反应20 min,再与芳胺于25℃反应3 h,合成了10个N-取代肉桂酰胺(3a~3j),产率85.8%~96.5%,其结构经1H NMR,13C NMR, IR和EI-MS确证。提出了DMAc促进反应的可能机理。
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