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苄氧基-双(N,N-二异丙基氨基)膦合成方法的改进

Synthesis of benzyloxy-bis(N,N-diisopropylamino) phosphine
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摘要 在石油醚中,三氯化磷依次与二异丙基胺和苯甲醇反应,通过“一锅法”制备了磷脂化学中用途广泛的磷脂酰化试剂苄氧基-双(N,N-二异丙基氨基)膦。产物通过减压蒸馏纯化,以三氯化磷计,总收率达87.4%。工艺简单,重复性好,适合大量制备。 The phosphatidylative reagent benzyloxy-bis(N, N-diisopropyl-amino) phosphine used widely in phosphatide chemistry was prepared by "one-pot" method. It was synthesized from PCl3 via reaction with i-Pr2NH and BnOH successively in petroleum ether. The product was purified by distillation in vacuum. The total yield was 87.4% based on PCl3. The preparative method was advantageous in synthesis in large scale due to its simplicity and reproducibility.
作者 岳智洲
出处 《化学试剂》 CAS CSCD 北大核心 2006年第4期245-246,共2页 Chemical Reagents
关键词 磷脂酰化试剂 苄氧基-双(N N-二异丙基氨基)膦 三氯化磷 phosphatidylative reagent benzyloxy-bis(N, N-diisopropylamino) phosphine phosphorus trichloride
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