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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35499Generated: October 29, 2026

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

https://huagongshe.com/reaction/35499

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 (Compound No. 62) M.P., 70.5°-72° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04767446
Source datasetuspto-grants-1988_08
ORD IDord-e3173e68cf8b4fb9acc3f8184e38fddf
Source noteuspto-grants-1988_08