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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 925428Generated: October 31, 2026

Triethylamine → HCID 89894133, compound

https://huagongshe.com/reaction/925428

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantSodium methanethiolateHCID 4378561—
ReactantHCID 89894011HCID 89894011—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 89894133HCID 8989413392%

Reaction Steps

To a turbid solution of (S)-tert-butyl 5-(hydroxymethyl)-2-oxooxazolidin-3-ylcarbamate (800 mg, 3.44 mmol) in DCM (5 mL), triethylamine (436 mg, 4.31 mmol) and methanesulfonyl chloride (493 mg, 4.31 mmol) were added and the reaction was stirred, at r.t., under nitrogen for 1 h 30 min. Conversion into the corresponding methanesulfonyl intermediate was complete. The solution was washed with cold citric acid (pH=4-5) and cold brine and the organic layer was separated and dried over Na2SO4. Evaporation of the solvent at 32° C. yielded a colourless foam (980 mg; yield=92%) that was dissolved in DMF (5 mL). Sodium methanethiolate (302 mg, 4.31 mmol) was added and the mixture stirred at 60° C. for 1 h. Conversion into the title product was complete. AcOEt was added and the solution was washed with cold citric acid (pH=3-4), then cold water and cold brine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09284306B2
Source datasetuspto-grants-2016_03
ORD IDord-06ce2b53b9f84d64a77af18f76afb419
Source noteuspto-grants-2016_03