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Acta Chimica Sinica ›› 2002, Vol. 60 ›› Issue (9): 1571-1574. Previous Articles Next Articles
Original Articles
顾彦龙;杨宏洲;邓友全
发布日期:
Gu Yanlong;Yang Hongzhou;Deng Youquan
Published:
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The synthesis of benzyl acetate by sodium acetate and benzyl chloride was investigated in various 1,3-dialkylimidazolium and alkylpyridium ionic liquids. 1-Alkyl-3-methylimidazolium tetrafluoroborate ([C_nMIm][BF_4]) ionic liquids were found to be an effective solvent and catalyst for the reaction. When the reaction was performed at 60 ℃, the molten sodium acetate was miscible with 1- ethyl-3-methylimidazolium tetrafluoroborate ionic liquid but the product benzyl acetate was not. Therefore, the products could be conveniently separated by decantation. The benzyl acetate yield was as high as 90% with >99% purity. The ionic liquid could be reused for several times and did not lose the catalytic activity.
Key words: GLYOXALINE P, PYRIDINE P, SODIUM ACETATE, CHLOROMETHYLBENZENE, benzyl acetate, CATALYTIC REACTION
CLC Number:
O643
Gu Yanlong;Yang Hongzhou;Deng Youquan. Catalytic Synthesis of Benzyl Acetate from Sodium Acetate and Benzyl Chloride in Room Temperature Ionic Liquid[J]. Acta Chimica Sinica, 2002, 60(9): 1571-1574.
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