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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1534174Generated: October 26, 2026

Trifluoroacetic acid → 2-(2-Fluoroethylthio)-phenylsulfonamide

https://huagongshe.com/reaction/1534174

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant2-(2-fluoroethylthio)-N-tert.-butylphenylsulfonamideHCID 19910936—
SolventChloroformHCID 6212—
Product2-(2-Fluoroethylthio)-phenylsulfonamideHCID 19809754—

Reaction Steps

25 ml of trifluoroacetic acid are added at a temperature of 0° C. to a solution of 3.88 g of 2-(2-fluoroethylthio)-N-tert.-butylphenylsulfonamide, obtained in accordance with Example P1, in 25 ml of trichloromethane. After stirring for 18 hours at a temperature of +25° C., the resulting brown reaction mixture is lyophilised. After chromatographic purification of the oily residue with 1) ethyl acetate/petroleum ether (1:1) over silica gel and 2) dichloromethane/acetone (9:1) over silica gel, the resulting fractions are concentrated by evaporation to give 1.5 g (60.5% of the theoretical yield) of crystalline 2-(2-fluoroethylthio)-phenylsulfonamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05087749
Source datasetuspto-grants-1992_02
ORD IDord-8c7a26a5f0f042409d8bf6feb52d9d17
Source noteuspto-grants-1992_02