HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 643281Generated: October 28, 2026
Sodium borohydride → (5-Bromopyridin-2-yl)methanol
https://huagongshe.com/reaction/643281
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 5-Bromopyridine-2-carbaldehyde | HCID 9877562 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (5-Bromopyridin-2-yl)methanol | HCID 5200169 | — |
Reaction Steps
The 5-bromo-pyridine-2-carbaldehyde (2.0 g) was taken up in MeOH and cooled to 0° C. Sodium borohydride (450 mg) was added in portions at 0° C. The solution was warmed to 25° C. and stirred at that temperature for 1.5 h. The solution was concentrated, and the residue was quenched with 1 M HCl(aq.). The solution was stirred at 25° C. for 0.5 h. The solution was rendered basic via addition of solid K2CO3. The mixture was extracted with CH2Cl2. The combined organic layers were dried (MgSO4), filtered, and concentrated to give (5-bromo-pyridin-2-yl)-methanol as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07700597B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-8c0eefc32a6f4683815a241cef35359e |
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| Source note | uspto-grants-2010_04 |
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