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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1798845Generated: November 3, 2026

Water → tert-Butyl N-(2-((methylsulfonyl)oxy)ethyl)carbamate

https://huagongshe.com/reaction/1798845

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactanttert-butyl N-(2-hydroxyethyl)carbamateHCID 2733206—
SolventDichloromethaneHCID 6344—
Producttert-Butyl N-(2-((methylsulfonyl)oxy)ethyl)carbamateHCID 22605302—

Reaction Conditions

Temperature0 °C

Reaction Steps

1 g (6.2 mmol) tert.-butyl (2-hydroxyethyl)carbamate and 0.75 g (7.44 mmol) triethylamine are dissolved in 250 ml dichloromethane and the solution is cooled to 0° C. 0.78 g (6.82 mmol) methanesulfonyl chloride are added slowly. The reaction mixture is stirred at 0° C. for one hour, then water is added, and the aqueous phase is extracted three times with ethyl acetate. The combined organic phases are dried over sodium sulfate, evaporated to dryness in vacuo, and the crude product is purified by column chromatography (silica, eluent: cyclohexane/ethyl acetate 5:1→2:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08343987B2
Source datasetuspto-grants-2013_01
ORD IDord-dadffe2f642f47939d1da51bdf712ab3
Source noteuspto-grants-2013_01