Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 853774Generated: October 26, 2026

4-Chlorobenzenesulfonyl chloride → 2,2,2-Trifluoroethane-1-sulfonamide

https://huagongshe.com/reaction/853774

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chlorobenzenesulfonyl chlorideHCID 7398—
ReactantTriethylamineHCID 8471—
Reactant1-(2,2,2-Trifluoroethyl)piperidineHCID 17840004—
Solvent1,2-DichloroethaneHCID 11—
Product2,2,2-Trifluoroethane-1-sulfonamideHCID 21265546114.1%

Reaction Steps

To a solution of O-protected trifluoroethyl piperidine (1.13 g, 3.6 mmol) in DCE (15 mL) was added triethylamine (0.6 mL, 4.3 mmol) then 4-chlorobenzenesulfonyl chloride (1.13 g, 5.4 mmol) and the reaction mixture was heated at reflux overnight. The final mixture was concentrated and directly purified by flash chromatography over silica gel (eluting with hexane to DCM) to afford 0.67 g (38%) of O-protected trifluoroethyl sulfonamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07256186B2
Source datasetuspto-grants-2007_08
ORD IDord-6f48be7f0b274a12b71403a5aec730ef
Source noteuspto-grants-2007_08