HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → (5-Bromopyridin-2-yl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Methyl 5-bromopyridine-2-carboxylate | HCID 7016458 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (5-Bromopyridin-2-yl)methanol | HCID 5200169 | — |
Reaction Steps
Methyl 5-bromopyridine-2-carboxylate (2.00 g, 9.27 mmol) was dissolved in ethanol (20.0 mL). Sodium borohydride (1.05 g, 27.8 mmol) was added at 0° C., and the mixture was stirred at room temperature for 18 h. The mixture was then concentrated under reduced pressure, quenched with 1 N hydrochloric acid, neutralized with solid potassium carbonate and extracted with dichloromethane. The organic layer was dried over magnesium sulfate and evaporated to give 1.57 g (90% of th.) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09040691B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-da26f20938424b4e8d715b0b9da26a96 |
| Source note | uspto-grants-2015_05 |