Diflunisal was prepared from 2,4 difluoroaniline via biphenylation,Friedel Crafts acylation,Baeyer Villiger rearrangement,hydrolysis and carboxylation. The overall yield was 38.4%.

 
  • 以 2 ;4-二氟苯胺为起始原料 ;经联苯化作用、Friedel-Crafts酰化反应、Baeyer-Villiger重排、水解和羧基化作用 5步反应制得 2′;4′-二氟 -4-羟基 -(1 ;1′-联苯 ) -3 -羧酸 ;总收率可达 3 8.;4%25
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