HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → (3-Fluoropyridin-2-yl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 3-Fluoro-2-pyridinecarboxaldehyde | HCID 11344017 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (3-Fluoropyridin-2-yl)methanol | HCID 19703803 | 93% |
Reaction Steps
A solution of 2-formyl-3-fluoropyridine (4.0 g, 32 mmol) and sodium borohydride (309 mg, 8 mmol) in absolute ethanol (40 mL) was stirred at 0° C. for 15 minutes and at room temperature for 1 hour. The reaction was quenched with saturated aqueous ammonium chloride (5 mL) and filtered through diatomaceous earth to remove solids. The filtrate was evaporated and the resultant white solid was dissolved in ethyl acetate and water. The aqueous layer was extracted with ethyl acetate (5×30 mL) and the combined extracts were dried over anhydrous sodium sulfate. Solvent removal provided 3.78 g (93%) of the titled product as a pale yellow oil:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05593993 |
| Source dataset | uspto-grants-1997_01 |
| ORD ID | ord-fdf34a2ef3d04e6db937db8c77af126e |
| Source note | uspto-grants-1997_01 |