HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(3-Bromo-4-fluorophenyl)ethan-1-one → 1-(3-Bromo-4-fluorophenyl)ethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(3-Bromo-4-fluorophenyl)ethan-1-one | HCID 70508 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(3-Bromo-4-fluorophenyl)ethanol | HCID 20785306 | — |
Reaction Steps
A solution of 1-(3-bromo-4-fluorophenyl)ethanone (15.0 g, 69 mmol) in tetrahydrofuran (200 mL) was treated with sodium borohydride (5.3 g, 138 mmol) at 0° C. After the addition, the ice bath was removed, and the mixture was stirred at room temperature for 30 minutes and at reflux overnight. After cooling, 1N HCl (10 mL) was slowly added and the reaction mixture was concentrated. The residue was partitioned between ethyl acetate and brine. The organic phase was washed with water, and concentrated. The residue was purified by flash chromatography (30% ethyl acetate in hexane) to provide the title compound. MS (DCI/NH3) m/z 220 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08466150B2 |
| Source dataset | uspto-grants-2013_06 |
| ORD ID | ord-17f818d0fe3f4d93a8a48433303b2303 |
| Source note | uspto-grants-2013_06 |