HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cfc 113 → Benzene, [(2-chloro-1,1,2-trifluoroethyl)thio]-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cfc 113 | HCID 6428 | — |
| Reactant | Chlorotrifluoroethylene | HCID 6594 | — |
| Reactant | Thiophenol | HCID 7969 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Benzene, [(2-chloro-1,1,2-trifluoroethyl)thio]- | HCID 11806392 | — |
Reaction Steps
In 300 ml of dimethylformamide was dissolved 55 g of thiophenol, and 55 g of triethylamine was added to the solution. Trifluorochloroethylene was passed into the mixture over the period of 2 hours under heating with stirring at 60° C. (trifluorochloroethylene was generated by reacting 187 g of 1,1,2-trifluorotrichloroethane with 130 g of powdered zinc in ethanol in accordance with the conventional method). After the conclusion of the reaction, the reaction mixture was concentrated to dryness under reduced pressure, and the resulting oily material was distilled under reduced pressure to give 55 g of (1,1,2-trifluoro-2-chloroethyl)phenylsulfide as a colorless liquid having a boiling point of 52°-53° C./0.2 mmHg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04843100 |
| Source dataset | uspto-grants-1989_06 |
| ORD ID | ord-70ab298ae8d44303857bfdfbbcda3d5d |
| Source note | uspto-grants-1989_06 |