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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2230538Generated: October 30, 2026

Dichloromethane → 2-(Methylsulfonyl)ethyl methanesulfonate

https://huagongshe.com/reaction/2230538

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-(Methylsulfonyl)ethanolHCID 84834—
SolventWaterHCID 962—
Product2-(Methylsulfonyl)ethyl methanesulfonateHCID 18464597—

Reaction Steps

Combine 2-methylsulfonylethanol (7.7 g, 62 mmol) and dichloromethane (50 mL). Cool in an ice bath. Add methanesulfonyl chloride (7.81 g , 68.2 mmol). Add N,N-diisopropylethylamine (8.0 g, 62 mmol). After the addition of N,N-diisopropylethylamine, warm to ambient temperature. After 12 hours, add water and separate the layers. Extract the organic, layer and extract with a saturated aqueous sodium bicarbonate solution. Dry the organic layer over Na2SO4, filter and evaporate in vacuo to give the title compound: mp; 55-57° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06423704B1
Source datasetuspto-grants-2002_07
ORD IDord-899da5f138ef47d2adfab9d0f9418231
Source noteuspto-grants-2002_07