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 to 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 the petroleum ether (60°-80°) gave 1,1-diphenyl-2-chloro-ethan-1-ol (60%) as a white crystalline solid, m.p. 56°-57°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04880457 |
| Source dataset | uspto-grants-1989_11 |
| ORD ID | ord-c451265250e440e9b258937ea8190a54 |
| Source note | uspto-grants-1989_11 |