Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 129783Generated: October 25, 2026

Ethyl Methanesulfonate → Ethyl (diethoxyphosphoryl)methanesulfonate

https://huagongshe.com/reaction/129783

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl MethanesulfonateHCID 6113—
ReactantDiethyl chlorophosphateHCID 13139—
ReactantAmmonium ChlorideHCID 25517—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductEthyl (diethoxyphosphoryl)methanesulfonateHCID 1093420570%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05470845
Source datasetuspto-grants-1995_11
ORD IDord-33529eec5d4f4ebf99ed1915cc5ec481
Source noteuspto-grants-1995_11