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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1822061Generated: November 2, 2026

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

https://huagongshe.com/reaction/1822061

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 numberUS07608628B2
Source datasetuspto-grants-2009_10
ORD IDord-f1ca54da4036490c96bf4f54fdfc20cd
Source noteuspto-grants-2009_10