HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Bromo-2-fluorobenzaldehyde → (5-Bromo-2-fluorophenyl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Bromo-2-fluorobenzaldehyde | HCID 736327 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (5-Bromo-2-fluorophenyl)methanol | HCID 2773352 | 97.7% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
To a solution of 5-bromo-2-fluoro-benzaldehyde (6.10 g, 30.0 mmol) in 30 mL of THF at 0° C. is added 5 mL of sodium borohydride (2.0M solution in triglyme, 10.0 mmol). The reaction mixture is stirred at 0° C. for 25 min and then quenched by the addition of 1N HCl. The mixture is diluted with EtOAc and the layers are separated. The organic layer is washed with H2O and saturated NaCl. The organic layer is dried over MgSO4, filtered and concentrated. The crude product is purified by column chromatography eluting with 15% EtOAc/hexanes to afford the title compound (6.00 g, 29.3 mmol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05731315 |
| Source dataset | uspto-grants-1998_03 |
| ORD ID | ord-dfa8e518af0e4946b9f86e5f4d0e8666 |
| Source note | uspto-grants-1998_03 |