HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 1-(5-Bromo-2-chlorophenyl)ethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 1-(5-Bromo-2-chlorophenyl)ethan-1-one | HCID 13628145 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-(5-Bromo-2-chlorophenyl)ethanol | HCID 58762644 | 99.3% |
Reaction Steps
Sodium borohydride (1.182 g, 51.4 mmol) was added to a stirred solution of 1-(5-bromo-2-chlorophenyl)ethanone (10 g, 42.8 mmol) in methanol at 0° C., The resulting bubbling white mixture was allowed to warm to room temperature and stirred for 2 h. The reaction mixture was quenched with acetone (50 mL) and concentrated by rotary evaporation. The residue was partitioned between ethyl acetate and water. The organic phase was dried and concentrated to yield the title compound (10 g, 42.5 mmol, 99% yield) as a white solid: 1H NMR (CDCl3): δ 7.75 (d, 1H), 7.32 (m, 1H), 7.19 (m, 1H), 5.23 (q, 1H), 1.95 (d, 1H), 1.48 (d, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08609592B2 |
| Source dataset | uspto-grants-2013_12 |
| ORD ID | ord-8feae0ab500d4dbfb65229e4b782c8a7 |
| Source note | uspto-grants-2013_12 |