Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 466356Generated: October 29, 2026

Methyl iodide → N-(2-acetylphenyl)-N-methylmethanesulfonamide

https://huagongshe.com/reaction/466356

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantEthyl AcetateHCID 8857—
ReactantSodium hydrideHCID 24758—
ReactantN-(2-acetylphenyl)methanesulfonamideHCID 2767200—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
ProductN-(2-acetylphenyl)-N-methylmethanesulfonamideHCID 19873387—

Reaction Steps

2'-Acetylmethanesulfonanilide (1.0 g, 4.7 mmol) in 10 ml tetrahydrofuran is reacted with 0.23 g (4.8 mmol) of 50% sodium hydride dispersion in mineral oil at 5° C. for 15 min. Methyl iodide (1.5 g, 10.56 mmol) in 10 ml of dimethylformamide is added over 15 min at 0°-10° C. and stirred in cold for 15 min. Dimethylformamide (10 ml) is added, and the reaction is stirred for 2 days at room temperature. The reaction is taken up into ethyl acetate, the organic layer washed with water, sodium carbonate solution, water, and saturated sodium chloride successively. The dried organic layer is evaporated and the product crystallized from ether-pet. ether; m.p. 98°-99° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05155268
Source datasetuspto-grants-1992_10
ORD IDord-1b06c96958d546a188a3816ad364e196
Source noteuspto-grants-1992_10