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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1272521Generated: October 27, 2026

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

https://huagongshe.com/reaction/1272521

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

b)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 was heated at reflux overnight. The final mixture was concentrated and directly purified by flash chromatography over silica gel (eluting hexane to DCM) to afford 0.67 g (38%) of O-protected trifluoroethyl sulfonamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07208602B2
Source datasetuspto-grants-2007_04
ORD IDord-6120e816896744f9ae699066923ae09d
Source noteuspto-grants-2007_04