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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | 2-Chloro-1,1,1-trifluoroethane | HCID 6408 | — |
| Reactant | p-Chlorothiophenol | HCID 7815 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | p-Chlorophenyl(2,2,2-trifluoroethyl) sulfide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05534634 |
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| Source dataset | uspto-grants-1996_07 |
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| ORD ID | ord-bb55755f9c53499590108e3f74232cbc |
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| Source note | uspto-grants-1996_07 |
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