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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35500Generated: October 29, 2026

Tert-Butylamine → N-t-butyl-3-methyl-4-(trifluoromethanesulfonamido)benzenesulfonamide

https://huagongshe.com/reaction/35500

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-ButylamineHCID 6385—
ReactantHCID 13194853HCID 13194853—
SolventTetrahydrofuranHCID 8028—
ProductN-t-butyl-3-methyl-4-(trifluoromethanesulfonamido)benzenesulfonamideHCID 1319485434.3%

Reaction Steps

3-Methyl-4-(trifluoromethanesulfonamido)benzenesulfonyl chloride (1.5 g) was added to tetrahydrofuran (40 ml) containing t-butylamine (0.65 g), and the resultant mixture was allowed to stand at room temperature overnight. The reaction mixture was concentrated and extracted with chloroform. The extract was washed with 5% hydrochloric acid and water in order, dried over anhydrous magnesium sulfate and concentrated. The residue was recrystallized from benzene and then from toluene to give 0.57 g of N-t-butyl-3-methyl-4-(trifluoromethanesulfonamido)benzenesulfonamide (Compound No. 16). M.P., 139.5°-140.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04767446
Source datasetuspto-grants-1988_08
ORD IDord-efe5e0d0c4ae41938cfc06ca65b41b15
Source noteuspto-grants-1988_08