HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 3-Trifluoromethylbenzhydryl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 3-(Trifluoromethyl)benzhydrol | HCID 2777404 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 3-Trifluoromethylbenzhydryl chloride | HCID 596829 | 100% |
Reaction Steps
To a stirred mixture of 40 parts of sulfinyl chloride in 150 parts of trichloromethane is added dropwise a solution of 64 parts of α-phenyl-3-(trifluoromethyl)benzenemethanol in 375 parts of trichloromethane. Upon completion, stirring is continued for 1 hour at room temperature. The whole is heated to reflux and stirring is continued for 3 hours at reflux temperature. After stirring overnight at room temperature, the solvent is evaporated. The residue is taken up in methylbenzene and the latter is evaporated again, yielding 70 parts (100%) of 1-(chlorophenylmethyl)-3-(trifluoromethyl)benzene as an oily residue.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04082755 |
| Source dataset | uspto-grants-1978_04 |
| ORD ID | ord-83a79e8b53454c84ae64437917732ccd |
| Source note | uspto-grants-1978_04 |