HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 2-Chloro-1-cyclohexyl-4-(1,2,2-trichloroethyl)benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 21444217 | HCID 21444217 | — |
| Catalyst | Pyridine | HCID 1049 | — |
| Product | 2-Chloro-1-cyclohexyl-4-(1,2,2-trichloroethyl)benzene | HCID 21444251 | — |
Reaction Steps
β,β-Dichloro-α-(3-chloro-4-cyclohexylphenyl)ethanol (67.5 g.; 0.22 moles) is heated with thionyl chloride (110 ml) containing 1 drop of pyridine until solution is obtained. The heating is discontinued and the reaction is allowed to proceed at room temperature for 12 hours. The reaction mixture is heated for an additional hour and the thionyl chloride removed, chased by benzene several times and distilled to give β,β,α,3-tetrachloro-4-cyclohexylphenylethane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04016214 |
| Source dataset | uspto-grants-1977_04 |
| ORD ID | ord-1b1b38b352c649f697b1fab4b6c5226b |
| Source note | uspto-grants-1977_04 |