HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → HCID 22767075, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 2793934 | HCID 2793934 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 22767075 | HCID 22767075 | — |
Reaction Steps
290 g (0.985 mol) of 2-chlorophenyl-(biphenyl-4-yl)-carbinol are dissolved in 1,000 ml of benzene and a solution of 144 ml (2 mols) of thionyl chloride in 400 ml of benzene is added slowly at 40° C. with stirring. The reaction mixture is heated under reflux for 15 hours. The solvent is distilled off in vacuo and the residue is stirred with 500 ml of petroleum ether. The crystals produced are filtered off and purified by recrystallization from ethanol. 36 g (89% of theory) of (2-chlorophenyl)-(biphenyl-4-yl)-chloromethane [alternatively named as α-(biphenyl-4-yl)-2l -chlorobenzyl chloride] of melting point 80° C. are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04118487 |
| Source dataset | uspto-grants-1978_10 |
| ORD ID | ord-94f4803919aa46d0bdb97661df228760 |
| Source note | uspto-grants-1978_10 |