HuagongsheHuagongshe Chemistry Print Report · For research reference only
Borohydride → (2-Amino-5-bromo-3-chlorophenyl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Borohydride | HCID 28123 | — |
| Reactant | 2-Amino-5-bromo-3-chlorobenzoic acid | HCID 827979 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (2-Amino-5-bromo-3-chlorophenyl)methanol | HCID 67080684 | 82% |
Reaction Steps
To a solution of 2-amino-5-bromo-3-chlorobenzoic acid (13.0 g, 52.0 mmol) in THF (200 mL) was added borohydride in THF (300 mL, 1N) at ice/water bath, and the reaction mixture was stirred at room temperature overnight. The mixture was quenched with methanol (100 mL) and concentrated to a volume of 50 mL. The residue was diluted with aqueous sodium bicarbonate (400 mL) and extracted with ethyl acetate (200 mL×3). The organic layers were separated, combined, washed by brine (100 mL), dried over sodium sulfate, filtered and concentrated to afford the title product (10.0 g, 82%). MS (ES+) C7H7BrClNO requires: 234, 236, found: 236, 238 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09434700B2 |
| Source dataset | uspto-grants-2016_09 |
| ORD ID | ord-2c837e710ae1411eb1a34020b955fe70 |
| Source note | uspto-grants-2016_09 |