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HRID 129783作成日:2026年10月25日

Ethyl Methanesulfonate → Ethyl (diethoxyphosphoryl)methanesulfonate

https://huagongshe.com/reaction/129783

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl MethanesulfonateHCID 6113—
反応物Diethyl chlorophosphateHCID 13139—
反応物Ammonium ChlorideHCID 25517—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
溶媒HexaneHCID 8058—
生成物Ethyl (diethoxyphosphoryl)methanesulfonateHCID 1093420570%

反応手順

A solution of ethyl methanesulfonate (4.27 mL, 40.3 mmol) in 100 mL of dry THF was treated at -78° C. with 19.3 mL (44.4 mmol) of n-BuLi in hexane. After 15 min. diethyl chlorophosphate (3.30 ml, 22.2 mmol) was added. The solution was kept at -78° C. for 0.5 h and allowed to stay at -50° C. for 1 h. Saturated ammonium chloride (75 mL) was added to the solution and the mixture warmed to room temperature. The mixture was concentrated (THF removed), diluted with water and extracted with methylene chloride (3×70 mL). The combined organic fractions were dried (MgSO4), concentrated and purified by distillation to yield 3.86 g (70%) of title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05470845
出典データセットuspto-grants-1995_11
ORD IDord-33529eec5d4f4ebf99ed1915cc5ec481
出典メモuspto-grants-1995_11