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首页> 外文期刊>Synlett >Facile Two-Step Synthesis of Methyl Bis(2,2,2-trifluoroethyl)phosphonoacetate by Exploiting Garegg–Samuelsson Reaction Conditions
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Facile Two-Step Synthesis of Methyl Bis(2,2,2-trifluoroethyl)phosphonoacetate by Exploiting Garegg–Samuelsson Reaction Conditions

机译:通过利用Garegg-Samuelsson反应条件,容易两步合成甲基双(2,2,2-三氟乙基)膦酸乙酯

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摘要

A facile two-step synthesis of methyl bis(2,2,2-trifluoroethyl)phosphonoacetate (Still–Gennari reagent) has been developed by exploiting Garegg–Samuelsson reaction conditions. Starting from trimethyl phosphonoacetate, Still–Gennari reagent was prepared in 94% yield via methyl 2-{bis[(trimethylsilyl)oxy]phosphoryl}acetate intermediate. This synthetic procedure was also used to prepare some kinds of Horner–Wadsworth–Emmons reagents and related compounds.
机译:通过利用Garegg-Samuelsson反应条件开发了甲基双(2,2,2-三氟乙基)膦酰基(静止 - 甘露乙基)膦酰乙酸酯(仍然是-GeNnari试剂)的容易两步合成。 从三甲基膦酰基乙酸酯开始,通过甲基2-·(三甲基甲硅烷基)氧丙酯中间体,以94%产率以94%收率制备。 该合成程序还用于制备某些类型的Horner-Wadsworth-Emmons试剂和相关化合物。

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