HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroform → 7-Trifluoromethyl-8,10-dichloro-10,11-dihydrodibenzo(b,f)thiepine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | (2-{[4-Chloro-3-(trifluoromethyl)phenyl]sulfanyl}phenyl)methanol | HCID 12374606 | — |
| Product | 7-Trifluoromethyl-8,10-dichloro-10,11-dihydrodibenzo(b,f)thiepine | HCID 12374624 | — |
Reaction Steps
A mixture of the alcohol from the preceding experiment (3.3 g) and thionyl chloride (1.2 ml) is allowed to stand at room temperature for 12 hours and then heated under a reflux condenser in a steam-bath for 1 hour. The reaction mixture is cooled, dissolved in chloroform and the solution washed with water and dried over calcium chloride. Evaporation of the solvent affords crystalline 7-trifluoromethyl-8,10-dichloro-10,11-dihydrodibenzo(b,f)thiepine, melting at 100°-102° C. after crystallization from acetone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04238611 |
| Source dataset | uspto-grants-1980_12 |
| ORD ID | ord-d62f93ef8f1649088421046c2c9926d3 |
| Source note | uspto-grants-1980_12 |