HuagongsheHuagongshe Chemistry Print Report · For research reference only
Borohydride → (2-Amino-5-bromo-4-chlorophenyl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Borohydride | HCID 28123 | — |
| Reactant | 2-Amino-5-bromo-4-chlorobenzoic acid | HCID 19612050 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (2-Amino-5-bromo-4-chlorophenyl)methanol | HCID 67081018 | 71% |
Reaction Steps
To a solution of 2-amino-5-bromo-4-chlorobenzoic acid (9.0 g, 36.0 mmol) in THF (150 mL) was added borohydride in THF (144 mL, 1 M) at room temperature, and the reaction mixture was stirred overnight. The reaction mixture was quenched with methanol (50 mL), and concentrated to a volume of 50 mL. The residue was diluted with water (100 mL) and extracted with ethyl acetate (150 mL×3). The organic layers were separated, combined, washed with water (100 mL) and brine (100 mL), dried over sodium sulfate, filtered and concentrated to afford the title compound (crude, 6 g, 71%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09434700B2 |
| Source dataset | uspto-grants-2016_09 |
| ORD ID | ord-077a42d133124a1b9775569963818e3b |
| Source note | uspto-grants-2016_09 |