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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1015705Generated: October 30, 2026

3-Cyanobenzene-1-sulfonyl chloride → 3-(aminomethyl)-N-methylbenzenesulfonamide

https://huagongshe.com/reaction/1015705

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Cyanobenzene-1-sulfonyl chlorideHCID 2801360—
ReactantMonomethylamine methanolHCID 57454252—
Product3-(aminomethyl)-N-methylbenzenesulfonamideHCID 16785597—

Reaction Steps

(Step 1) To a 40% methylamine methanol solution (5 ml) was added 3-cyanobenzenesulfonyl chloride (0.88 g) at 0° C., and the mixture was stirred at room temperature for 2 hr. The solvent was evaporated under reduced pressure, saturated brine was added, and the mixture was extracted with ethyl acetate. The solvent was evaporated under reduced pressure. 10% Palladium carbon powder (0.46 g) was added to a solution (10 ml) of the residue in ethanol, and the mixture was stirred overnight under a hydrogen atmosphere (1 atm). The solution was filtered through celite. The solvent was evaporated under reduced pressure. The residue was purified by basic silica gel column chromatography (ethyl acetate) to give 3-(aminomethyl)-N-methylbenzenesulfonamide (0.38 g) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07985862B2
Source datasetuspto-grants-2011_07
ORD IDord-a1058a9bdc7a4306b79a01872932daed
Source noteuspto-grants-2011_07