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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 655906Generated: October 30, 2026

Methanesulfonyl chloride → N-(2-oxo-2-phenylethyl)methanesulfonamide

https://huagongshe.com/reaction/655906

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantEthanone, 2-amino-1-phenyl-, hydrochloride (1:1)HCID 2723597—
SolventDimethylformamideHCID 6228—
ProductN-(2-oxo-2-phenylethyl)methanesulfonamideHCID 2189354198.5%

Reaction Steps

To a solution of 2-amino-1-phenylethanonehydrochloride (1a) (1715 mg, 10 mmol) in DMF (20 mL) was added TEA (2.8 mL, 20 mmol). Upon cooling under ice-water bath, methylsulfonyl chloride (0.77 mL, 10 mmol) was added slowly and the reaction mixture stirred at RT for 12 h. The mixture was partitioned between dichloromethane and brine, dried over sodium sulfate and then concentrated in vacuo to give the title compound (2100 mg, 98%) as an off white solid. MS APCI, m/z=214 (M+1). LCMS: 1.19 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08071621B2
Source datasetuspto-grants-2011_12
ORD IDord-6870b5d4ff464aff9ce5098715733885
Source noteuspto-grants-2011_12