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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1186441Generated: October 26, 2026

Tert-Butylamine → 2,2,2-Trifluoroethane-1-sulfonamide

https://huagongshe.com/reaction/1186441

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-ButylamineHCID 6385—
Reactant2,2,2-Trifluoroethanesulfonyl chlorideHCID 74242—
SolventTetrahydrofuranHCID 8028—
Product2,2,2-Trifluoroethane-1-sulfonamideHCID 2126554625.3%

Reaction Steps

Tetrahydrofuran (6 mL) was added to tert-butylamine (220 mg, 3.0 mmol), and 2,2,2-trifluoroethanesulfonyl chloride (300 mg, 1.6 mmol) was slowly added dropwise thereto. The mixture was stirred at room temperature for 30 minutes, and the solvent was evaporated off under reduced pressure. To the residue, trifluoroacetic acid (3.3 mL) was added and the mixture was stirred at room temperature for 15 hours. The solvent was evaporated off under reduced pressure, and purification by silica gel column chromatography (chloroform/methanol=100/0 to 5/1) was performed to give 2,2,2-trifluoroethanesulfonamide (Compound GC) (66 mg, yield: 25%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673908B2
Source datasetuspto-grants-2014_03
ORD IDord-f51f5d34c54742c5b261a348096b4291
Source noteuspto-grants-2014_03