HuagongsheHuagongshe Chemistry Print Report · For research reference only
4'-Bromo-3-chloropropiophenone → 4-Bromo-alpha-(2-chloroethyl)benzenemethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4'-Bromo-3-chloropropiophenone | HCID 95790 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Bromo-alpha-(2-chloroethyl)benzenemethanol | HCID 10800638 | — |
Reaction Steps
To a solution of 1-(4-Bromo-phenyl)-3-chloro-propan-1-one (1 g, 4.04 mmol) in tetrahydrofuran (9 ml) and water (0.58 ml) was added sodium borohydride (0.16 g, 4.28 mmol). The reaction mixture was stirred at room temperature for 2 hours, quenched with careful addition of water and extracted with ethyl acetate. The organic layers were separated, dried (MgSO4), filtered and concentrated to afford the title compound, which was used in the next step without further purification. LC/MS. (PS-A2) Rt 3.07 [M+H]+ No Ionization.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09283226B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-b87c609e7f384a9fb6fc0d8a434a7e94 |
| Source note | uspto-grants-2016_03 |