HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → (6-Chloro-2-methylpyridin-3-yl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 6-Chloro-2-methylpyridine-3-carbaldehyde | HCID 44754867 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (6-Chloro-2-methylpyridin-3-yl)methanol | HCID 59525984 | — |
Reaction Steps
Sodium borohydride (0.73 g, 19.28 mmol) was added to a solution of 6-chloro-2-methylnicotinaldehyde (1.5 g, 9.64 mmol) in methanol (38.6 mL) at room temperature. The mixture was stirred for 2 hours, then quenched with water and saturated aqueous sodium bicarbonate, and extracted three times with ethyl acetate. The organic layers were combined, dried over magnesium sulfate, filtered, and concentrated under reduced pressure to afford the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08367706B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-793b09812c5f4bde9dc40ab0690a36f3 |
| Source note | uspto-grants-2013_02 |