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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2200571Generated: October 30, 2026

Methanesulfonyl chloride → 2-(2-Ethyl-1,3-dioxolan-2-yl)ethyl methanesulfonate

https://huagongshe.com/reaction/2200571

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant2-(2-Ethyl-1,3-dioxolan-2-yl)ethan-1-olHCID 13940368—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product2-(2-Ethyl-1,3-dioxolan-2-yl)ethyl methanesulfonateHCID 88895626140.2%

Reaction Steps

To a solution of 2-(2-ethyl-1,3-dioxolan-2-yl)ethanol (233 mg, 1.59 mmol) and TEA (327 mg, 3.2 mmol) in DCM (10 mL) was added methanesulfonyl chloride (0.23 ml, 2.92 mmol) at 0° C. The resulting mixture was stirred at room temperature for 3 h. The mixture was diluted with DCM and water, and the phases were separated. The organic phase was washed with brine, dried over sodium sulfate, filtered and concentrated to give 2-(2-ethyl-1,3-dioxolan-2-yl)ethyl methanesulfonate (500 mg, 100%) as yellow oil that was used without purification. Product tlc [DCM/methanol (100:1) developed with potassium permanganate, Rf 0.6]

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09359359B2
Source datasetuspto-grants-2016_06
ORD IDord-56c32ec957044d3b8751658b7d1958dd
Source noteuspto-grants-2016_06