HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → [2-Fluoro-3-(trifluoromethoxy)phenyl]methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2-Fluoro-3-(trifluoromethoxy)benzaldehyde | HCID 45933730 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | [2-Fluoro-3-(trifluoromethoxy)phenyl]methanol | HCID 15582606 | 96% |
Reaction Steps
To a stirred solution of 2-fluoro-3-(trifluoromethoxy)benzaldehyde (1.00 g, 4.81 mmol) in methanol (20 mL) is added Sodium borohydride (0.36 g, 9.61 mmol) at 0° C. After stirring at room temperature for 16 hours, the reaction mixture is quenched with water. The mixture is diluted with ethyl acetate (100 mL) and washed with water. The organic layer is dried over sodium sulfate, and concentrated under reduced pressure to give 0.97 g (96% yield) of the title compound as colorless syrup. This material is used for the next reaction (Step-2) without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09302991B2 |
| Source dataset | uspto-grants-2016_04 |
| ORD ID | ord-6a82fb37a746443e8192358170810466 |
| Source note | uspto-grants-2016_04 |