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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35497Generated: October 29, 2026

Hydrochloric Acid → N-methyl-2,4-dimethyl-5-(trifluoromethanesulfonamido)benzenesulfonamide

https://huagongshe.com/reaction/35497

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethylamineHCID 6329—
ReactantHCID 13300558HCID 13300558—
SolventWaterHCID 962—
ProductN-methyl-2,4-dimethyl-5-(trifluoromethanesulfonamido)benzenesulfonamideHCID 1330055974.5%

Reaction Steps

A mixture of 2,4-dimethyl-5-(trifluoromethanesulfonamido)benzenesulfonyl chloride (1.5 g), a 40% aqueous soltution of methylamine (1 g) and water (20 ml) was stirred at room temperature and allowed to stand overnight at the same temperature. The resultant mixture was made acidic with 5% aqueous hydrochloric acid to precipitate an oily substance, which was then extracted with chloroform. The organic layer was washed with a 5% aqueous solution of hydrochloric acid and water in order and dried over anhydrous magnesium sulfate, followed by concentration. The residue was allowed to stand to give crytals, which were recrystallized from toluene to give 1.1 g of N-methyl-2,4-dimethyl-5-(trifluoromethanesulfonamido)benzenesulfonamide (Compound No. 29). M.P., 134.5°-135.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04767446
Source datasetuspto-grants-1988_08
ORD IDord-66aedee05ec645c69a89c17fb21802a0
Source noteuspto-grants-1988_08