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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1734738Generated: October 27, 2026

Carbon Dioxide → p-Chlorophenyl(2,2,2-trifluoroethyl) sulfide

https://huagongshe.com/reaction/1734738

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
Reactant2-Chloro-1,1,1-trifluoroethaneHCID 6408—
Reactantp-ChlorothiophenolHCID 7815—
ReactantSodium hydrideHCID 24758—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Productp-Chlorophenyl(2,2,2-trifluoroethyl) sulfideHCID 15634476—

Reaction Steps

A two-necked flask having a dry ice condenser fitted on top was charged with 50 ml of dry dimethylformamide and 2 g of a 60% strength by weight suspension of sodium hydride in paraffin, and subsequently 7.3 g of 4-chlorothiophenol in 10 ml of dimethylformamide were added dropwise. Chlorotrifluoroethane was then passed in at a reaction temperature of about 60° C., until the gas began to condense in the dry ice condenser. The mixture was stirred for a further 5 hours and the course of the reaction was monitored by thin-layer chromatography (silica gel; ethyl acetate/petroleum ether 1/5). The reaction mixture was worked up by pouring into water and extracting with dichloromethane. The combined organic extracts were dried and the solvent was distilled off at reduced pressure. The oily residue was subsequently distilled (43°-45° C./0.1 mbar), giving 8.8 g of 4-chloro(2',2',2'-trifluoroethylthio)benzene

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05534634
Source datasetuspto-grants-1996_07
ORD IDord-bb55755f9c53499590108e3f74232cbc
Source noteuspto-grants-1996_07