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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 727494Generated: October 25, 2026

Diethyl chlorophosphate → Isopropyl (Diethoxyphosphoryl)methanesulfonate

https://huagongshe.com/reaction/727494

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl chlorophosphateHCID 13139—
ReactantIsopropyl methanesulfonateHCID 13551—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductIsopropyl (Diethoxyphosphoryl)methanesulfonateHCID 1572597567%

Reaction Conditions

Temperature-40 °C

Reaction Steps

To a rapidly stirred solution of 8.28 g (60 mmol) of isopropyl methanesulfonate in 150 mL of THF at -73° C. (internal temp.) was added 25 mL (60 mmol) of 2.4M n-butyllithium dropwise over 20 min. The internal temperature was not allowed to rise above -69° C. throughout the course of the addition. After an additional 15 min., 5.17 g (30 mmol) of freshly distilled diethyl chlorophosphate was added at a rate to keep the solution temperature below -69° C. The reaction mixture was stirred for 0.3 h at -73° C. and for 0.5 h at -40° C. when it was quenched with 125 mL of saturated NH4Cl solution. The reaction mass was warmed to room temperature and the THF removed under reduced pressure. The remainder was partitioned between methylene chloride and water (3×75 mL). The extracts were dried (Na2SO4), concentrated, and purified by flash chromatography (350 g silica gel) eluting with 1:1 methylene chloride/ether to provide 5.20 g (67%) of title compound as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05712396
Source datasetuspto-grants-1998_01
ORD IDord-595cfc84a1e44c3f97b7e9e63e460877
Source noteuspto-grants-1998_01