HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 4-Bromo-2-fluoro-5-(hydroxymethyl)phenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2-Bromo-4-fluoro-5-hydroxybenzaldehyde | HCID 86636454 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-Bromo-2-fluoro-5-(hydroxymethyl)phenol | HCID 66726435 | 99.4% |
Reaction Steps
A solution of 2-bromo-4-fluoro-5-hydroxybenzaldehyde (2.0 g, 9.1 mmol) in MeOH (15 mL) was cooled in an ice bath before treatment of NaBH4 (390 mg, 10.3 mmol). After the complete addition of NaBH4, the reaction mixture was allowed to stir for 1 h at room temperature before it was quenched with equal volume of water. EtOAc (20 mL) was added to the reaction solution and the layers were separated. The aqueous layer was further extracted with equal volume of EtOAc before the organic layers were combined and dried over anhydrous Na2SO4 and filtered. The solvent was removed under reduced pressure. The residue was purified by silica gel column using Combiflash to give 4-bromo-2-fluoro-5-(hydroxymethyl)phenol (2.0 g, 83%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09145429B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-72a30117f81547ddaff279001a22f002 |
| Source note | uspto-grants-2015_09 |