Pentacoordinate Organosilicate-Catalyzed Michael Addition of β-Keto Esters to 3-Buten-2-one
作者:Jun-ichi Tateiwa、Akira Hosomi
DOI:10.1002/1099-0690(200104)2001:8<1445::aid-ejoc1445>3.0.co;2-q
日期:2001.4
The Michael addition of β-keto esters to 3-buten-2-one (methyl vinyl ketone, MVK) in the presence of a pentacoordinate organosilicate was investigated. Ethyl 2-oxo-1-cyclohexanecarboxylate reacted with MVK in the presence of potassium bis(1,2-benzenediolato)phenylsilicate to furnish ethyl 2-oxo-1-(3-oxo-1-butyl)-1-cyclohexanecarboxylate in 96% isolated yield. Ethyl 2-oxo-1-cyclopentanecarboxylate,
研究了在五配位有机硅酸盐存在下,β-酮酯与 3-丁烯-2-酮(甲基乙烯基酮,MVK)的迈克尔加成反应。2-氧代-1-环己烷羧酸乙酯在双(1,2-苯二醇基)苯基硅酸钾存在下与MVK反应,得到96%的2-氧代-1-(3-氧代-1-丁基)-1-环己烷羧酸乙酯分离产量。2-氧代-1-环戊烷羧酸乙酯、2-氧代-1-环辛烷羧酸乙酯、2-甲基-3-氧代丁酸乙酯和2-乙基-3-氧代丁酸乙酯也在双(1,2 -benzodiolato)苯基硅酸盐以中等至良好的产率产生相应的1,4-加合物。在这些反应中,硅酸盐可能同时用作路易斯酸催化剂和布朗斯台德碱催化剂。