HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → (2-Fluoro-4-iodopyridin-3-yl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2-Fluoro-4-iodopyridine-3-carbaldehyde | HCID 9992328 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (2-Fluoro-4-iodopyridin-3-yl)methanol | HCID 11021396 | — |
Reaction Steps
0.72 g (19.2 mmol) of sodium borohydride is added to a solution of 4 g (16 mmol) of 2-fluoro-4-iodo-3-pyridinecarbaldehyde (described in J.O.C., 1993, 58, pp. 7832) in 100 ml of tetrahydrofuran. The mixture is stirred at room temperature for 4 hours and then hydrolysed. The reaction mixture is extracted with ethyl acetate. The organic phases are dried and concentrated to yield the expected product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06699876B2 |
| Source dataset | uspto-grants-2004_03 |
| ORD ID | ord-d094e11700ea421e989ed6c166b22473 |
| Source note | uspto-grants-2004_03 |