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作 者:YuanRuMENG YeDiGUAN
机构地区:[1]DepartmentofChemistry,PekingUniversity,Beijing100871 [2]StateKeyLaboratoryofElemento-OrganicChemistry,NankaiUniversity,Tianjin300071
出 处:《Chinese Chemical Letters》2002年第11期1039-1042,共4页中国化学快报(英文版)
摘 要:This paper provides a simple, convenient and mild condition method for -alkylation of g-butyrolactone. Three types of (E)-a-alkenyl-g-butyrolactone compounds were synthesized by condensation of corresponding aldehydes and g-butyrolactone, using MeONa and EtONa as base. Then the a-alkyl-g-butyrolactones were gained by reducing the former alkenyl compounds through catalytic transfer hydrogenation under Pd/C catalyst with sodium hypophosphite at room temperature.This paper provides a simple, convenient and mild condition method for -alkylation of g-butyrolactone. Three types of (E)-a-alkenyl-g-butyrolactone compounds were synthesized by condensation of corresponding aldehydes and g-butyrolactone, using MeONa and EtONa as base. Then the a-alkyl-g-butyrolactones were gained by reducing the former alkenyl compounds through catalytic transfer hydrogenation under Pd/C catalyst with sodium hypophosphite at room temperature.
关 键 词:Alkylation of -butyrolactone CONDENSATION catalytic transfer hydrogenation Pd / C-sodium hypophosphite.
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