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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 129783생성일: 2026년 10월 24일

Ethyl Methanesulfonate → Ethyl (diethoxyphosphoryl)methanesulfonate

https://huagongshe.com/ko/reaction/129783

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl MethanesulfonateHCID 6113—
반응물Diethyl chlorophosphateHCID 13139—
반응물Ammonium ChlorideHCID 25517—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물Ethyl (diethoxyphosphoryl)methanesulfonateHCID 1093420570%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05470845
출처 데이터셋uspto-grants-1995_11
ORD IDord-33529eec5d4f4ebf99ed1915cc5ec481
출처 메모uspto-grants-1995_11