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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1295708Generated: October 27, 2026

Dichloromethane → 2-Methoxyethyl methanesulfonate

https://huagongshe.com/reaction/1295708

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactant2-MethoxyethanolHCID 8019—
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
SolventWaterHCID 962—
Product2-Methoxyethyl methanesulfonateHCID 146293—

Reaction Steps

Methanesulfonyl chloride (15 g, 0.13 mol) was added to a mixture of 2-methoxy ethanol (10 g, 0.13 mol), triethylamine (26.5 g, 0.26 mol) and dichloromethane (150 g) at 0° C. After being stirred at room temperature overnight, water (100 g) was added to the reaction mixture. The layers were separated and the organic layer was concentrated in vacuo at room temperature. This gave 13.1 g (65%) of the title mesylate as an oil. 1H NMR analysis supports the stated structure. *Previously reported in Tetrahedron 1995, 51, 4867-4890.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07244722B2
Source datasetuspto-grants-2007_07
ORD IDord-5b6a18b538ce40ac9b7e3e2dea2c6f57
Source noteuspto-grants-2007_07