Chem. J. Chinese Universities ›› 1992, Vol. 13 ›› Issue (9): 1212.

• Articles • Previous Articles     Next Articles

Studies on the Selectively Protecting Groups of Hydroxyls in Sucrose

WU Hong-Qiao, LI Cui-Juan, WANG Shi-Yu   

  1. Department of Chemistry, Peking University, Beijing, 100871
  • Received:1991-09-09 Online:1992-09-24 Published:1992-09-24

Abstract: Reaction of sucrose with trialkyl orthoacetate,subsequent tritylation,acetylation,and detritylation afforded derivatives of sucrose acetate by selectively blocking specific hydroxyls in sucrose and 4-6 acetyl migration.The treatment of sucrose alkyl 4,6-orthoacetate hexaaeetate with water or alcohol in the presence of an acid catalyst afforded corresponding 2,3,6,1',3',4',6'-hepta-O-acetylsucrose and 2,3.1',3',4',6'-hexa-O-acetylsucrose.These derivatives of sucrose acetate were available from sucrochemical studies and have been developed as convenient intermediate for the synthesis of sucrose derivatives.

Key words: Sucrose acetate, Trialkyl orthoacetate, Sucrose aikyl 4,6-orthoacetate hexaacetate

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