HuagongsheHuagongshe Chemistry Print Report · For research reference only
Borohydride → (2-Amino-4-methoxyphenyl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Borohydride | HCID 28123 | — |
| Reactant | 2-Amino-4-methoxybenzoic acid | HCID 351010 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (2-Amino-4-methoxyphenyl)methanol | HCID 45090899 | — |
Reaction Steps
To a solution of 2-amino-4-methoxybenzoic acid (15.0 g, 89.8 mmol) in THF (300 mL) was added borohydride in THF (450 mL, 450 mmol) at 0° C., and the reaction mixture was stirred at RT overnight. LCMS showed the reaction was completed. The reaction was quenched with water (150 mL) and extracted with ethyl acetate (500 mL×3). The organic layers were separated, combined, washed with water (200 mL) and brine (200 mL), dried over sodium sulfate, filtered and concentrated to afford the title compound. MS (ES+) C8H11NO2 requires: 153. found: 154 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09340514B2 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-7f05f344974642fb9b518b15511e2729 |
| Source note | uspto-grants-2016_05 |