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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 547287Generated: October 31, 2026

Sodium methanethiolate → HCID 86064723, compound

https://huagongshe.com/reaction/547287

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium methanethiolateHCID 4378561—
Reactanttert-butyl N-{2-[2-(methanesulfonyloxy)ethoxy]ethyl}carbamateHCID 12106196—
SolventDimethylformamideHCID 6228—
ProductHCID 86064723HCID 8606472396.6%

Reaction Conditions

Temperature80 °C

Reaction Steps

A suspension of 2-{2-[(tert-butoxycarbonyl)amino]ethoxy}ethyl methanesulfonate (28 g, 99 mmol) and sodium thiomethoxide (8.3 g, 119 mmol) in N,N-dimethylformamide (DMF, 200 mL) was heated to 80° C. and maintained at that temperature until analysis by thin layer chromatography (TLC) indicated that the starting material had been consumed. The reaction mixture was allowed to cool to ambient temperature and was then quenched with water (200 mL). The reaction mixture was extracted with diethyl ether (2×200 mL). The combined extracts were washed sequentially with saturated aqueous sodium bicarbonate (100 mL) and brine (100 mL), dried over anhydrous sodium sulfate, filtered, and then concentrated under reduced pressure to provide 22.5 g of tert-butyl 2-[2-(methylthio)ethoxy]ethylcarbamate as a light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07939526B2
Source datasetuspto-grants-2011_05
ORD IDord-2956082bb87a4100ad483657a6379cc9
Source noteuspto-grants-2011_05