Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2359311Generated: November 3, 2026

Benzenesulfonamide → Benzamide, 2,4,5-trifluoro-N-(phenylsulfonyl)-

https://huagongshe.com/reaction/2359311

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonamideHCID 7370—
Reactant2,4,5-Trifluorobenzoic acidHCID 521170—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductBenzamide, 2,4,5-trifluoro-N-(phenylsulfonyl)-HCID 5804633868%

Reaction Steps

To a solution of 2,4,5-trifluorobenzoic acid (0.50 g, 2.8 mmol) in dichloromethane (5 mL) was added N-di-isopropylethylamine (1.8 mL, 1.3 g, 8.5 mmol), WSCDI (0.82 g, 4.2 mmol) and DMAP (0.52 g, 4.2 mmol). After 10 minutes phenylsulfonamide (0.45 g, 4.2 mmol) was added and the reaction left at room temperature for 18 hours. The reaction mixture was concentrated in vacuo and the residue purified by reverse phase chromatography using CH3CN/water as eluent (5:95-95/5 over 30 mins) to yield the title compound (0.60 g, 67%) as a white solid

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08685977B2
Source datasetuspto-grants-2014_04
ORD IDord-2ca7feea9c48460daf0c7d9824cec811
Source noteuspto-grants-2014_04