HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2207142Generated: October 30, 2026
3-Bromopyridine-4-carboxaldehyde → (3-Bromopyridin-4-yl)methanol
https://huagongshe.com/reaction/2207142
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Bromopyridine-4-carboxaldehyde | HCID 2762997 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (3-Bromopyridin-4-yl)methanol | HCID 46840038 | 100% |
Reaction Steps
To a solution of 3-bromo-4-pyridinecarboxaldehyde 3 (3.0 g, 16.2 mmol) in absolute methanol (40 mL) was added NaBH4 (0.736 g 19.5 mmol) at 0° C. The mixture was stirred at 0° C. for 2 hours under nitrogen. The solvent was then removed under vacuum. Water and ethyl acetate were added and the organic layer was washed with water, dried over Na2SO4 and evaporated under vacuum to afford the compound 4 (3.021 g, 100%) as a white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09376387B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-bb7c78d3d0b540f092a6812cd00b00eb |
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| Source note | uspto-grants-2016_06 |
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