HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanone, 1-(1,1'-biphenyl)-4-yl-2-chloro- → Benzyl Chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanone, 1-(1,1'-biphenyl)-4-yl-2-chloro- | HCID 69463 | — |
| Reactant | HCID 178418336 | HCID 178418336 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Benzyl Chloride | HCID 7503 | — |
| Product | Magnesium | HCID 5462224 | — |
Reaction Steps
115.3 g (0.5 mol) of 4-phenylphenacyl chloride are added portions to a solution of benzyl-magnesium chloride, obtained from 24.3 g (1 mol) of magnesium and 115 ml (1 mol) of benzyl chloride in 150 ml of diethyl ether. The reaction mixture is warmed under reflux for 90 minutes and then poured onto aqueous ammonium chloride solution. The ether phase is separated off, washed with water, dried over sodium sulphate and concentrated. The oil which remains is made to crystallise by stirring with petroleum ether. 50 g (31% of theory) of 2-(4-biphenylyl)-3-chloro-1-phenylpropan-2-ol of melting point 96° C. are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04381306 |
| Source dataset | uspto-grants-1983_04 |
| ORD ID | ord-ef97697eeb914fa89d4c10e0af364c10 |
| Source note | uspto-grants-1983_04 |