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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 333077Generated: October 25, 2026

Ethyl Methanesulfonate → Ethyl (diethoxyphosphoryl)methanesulfonate

https://huagongshe.com/reaction/333077

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl MethanesulfonateHCID 6113—
ReactantDiethyl chlorophosphateHCID 13139—
Reactantn-Butyl lithiumHCID 61028—
SolventTetrahydrofuranHCID 8028—
ProductEthyl (diethoxyphosphoryl)methanesulfonateHCID 10934205117.1%

Reaction Steps

A solution of ethyl methanesulfonate (4.14 mL, 40.2 mmol) in anhydrous tetrahydrofuran (100 ml) was cooled to −78° C. under a nitrogen atmosphere. N-Butyllithium (20 ml, 50.0 mmol) was added slowly in 7 minutes after which stirring was continued for 15 minutes. Diethyl phosphorochloridate (4.36 mL, 30.2 mmol) was added, the reaction mixture was stirred for 2.5 h, the cooling bath was removed and the mixture was allowed to reach room temperature. The reaction mixture was quenched with aqueous saturated ammonium chloride (150 ml) and the resulting mixture was extracted with EtOAc (2×100 ml). The combined extracts were dried over sodium sulfate and concentrated under reduced pressure to yield 9.20 g of a yellow oil. The oil was purified over silicagel (600 g) using a gradient of ethyl acetate (0-100%) in heptane to yield 1.75 g of the product (6.7 mol, 17%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08877934B2
Source datasetuspto-grants-2014_11
ORD IDord-40d13101437a4e78a60ba9d76cfe0aff
Source noteuspto-grants-2014_11