HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → (4-(Trifluoromethyl)pyridin-3-yl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 4-(Trifluoromethyl)pyridine-3-carbaldehyde | HCID 21354724 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (4-(Trifluoromethyl)pyridin-3-yl)methanol | HCID 18914105 | — |
Reaction Steps
To a solution of sodium borohydride (324 mg, 8.6 mmol) in methanol (20 mL) was added a solution of 4-(trifluoromethyl)pyridine-3-carbaldehyde (1.0 g, 5.7 mmol) in methanol (10 mL) at 0° C. The mixture was stirred for 1.5 hours at room temperature. The solvent was evaporated, water was added, and the mixture was extracted 3 times with ethyl acetate. The combined organic phases were washed with brine and dried over sodium sulfate. After evaporation of the solvent, [4-(trifluoromethyl)pyridin-3-yl)methanol was obtained as an oil (980 mg, 97% yield) and used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09315521B2 |
| Source dataset | uspto-grants-2016_04 |
| ORD ID | ord-427c761b862f4dacba8eb785a1d1beb7 |
| Source note | uspto-grants-2016_04 |