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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1284822Generated: October 31, 2026

Dimethylamine → N,N-dimethyl-2,4-dimethyl-3-(trifluoromethanesulfonamido)benzenesulfonamide

https://huagongshe.com/reaction/1284822

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamineHCID 674—
Reactant2,4-Dimethyl-3-(trifluoromethanesulfonamido)benzenesulfonyl chlorideHCID 13537890—
SolventTetrahydrofuranHCID 8028—
ProductN,N-dimethyl-2,4-dimethyl-3-(trifluoromethanesulfonamido)benzenesulfonamideHCID 1330059369.7%

Reaction Steps

2,4-Dimethyl-3-(trifluoromethanesulfonamido)benzenesulfonyl chloride (1.4 g) was added to tetrahydrofuran (20 ml) containing dimethylamine (0.6 g), and the resultant mixture was allowed to stand overnight at room temperature. The reaction mixture was concentrated, admixed with 5% hydrochloric acid and extracted with chloroform. The extract was washed with 5% hydrochloric acid and water in order, dried over anhydrous magnesium sulfate and concentrated to give an oily substance, which was purified by column chromatography with silica gel (150 ml) to give 1.0 g of N,N-dimethyl-2,4-dimethyl-3-(trifluoromethanesulfonamido)benzenesulfonamide. M.P., 70.5°-72° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04564386
Source datasetuspto-grants-1986_01
ORD IDord-52d8f37eff5a4fc0b547c090268cedcd
Source noteuspto-grants-1986_01