HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromobenzene → 2-chloro-1,1-diphenylethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromobenzene | HCID 7961 | — |
| Reactant | 2-Chloroacetophenone | HCID 10757 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Sodium | HCID 5360545 | — |
| Product | 2-chloro-1,1-diphenylethanol | HCID 232596 | 60% |
Reaction Steps
Bromobenzene (0.2 mol, 31.4 g) in sodium dry diethyl ether (200 ml) was added dropwise to magnesium (0.22 gram atoms, 5.3 g ). After all the magnesium had reacted, phenacyl chloride (0.1 mol, 15.5 g) in diethyl ether (100 ml) was added dropwise and the solution stirred at room temperature for 1 hour. The reaction mixture was poured into saturated ammonium chloride solution, washed with water (3×150 ml), and dried (Na2SO4). Removal of the ether gave a pale yellow oil which solidified on standing. Recrystallisation from petroleum ether (60°-80°) gave 1,1-diphenyl-2-chloroethan-1-ol (60%) as a white crystalline solid, m.p. 56°-57°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04551469 |
| Source dataset | uspto-grants-1985_11 |
| ORD ID | ord-c3199c8677c84bd0bafb899bd88e3dc2 |
| Source note | uspto-grants-1985_11 |