HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 423182Generated: October 25, 2026
Sodium borohydride → (3-Bromopyridin-2-yl)methanol
https://huagongshe.com/reaction/423182
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Methyl 3-bromo-2-pyridinecarboxylate | HCID 12828946 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (3-Bromopyridin-2-yl)methanol | HCID 14022521 | 62% |
Reaction Steps
3-Bromo-pyridine-2-carboxylic acid methyl ester (12.8 g, 59.2 mmol) is dissolved in methanol (150 mL) and cooled to 0° C. To the mixture is added NaBH4 (11.2 g, 296 mmol) in 1.0 g portions. The mixture is warmed to room temperature and stirred for 3 h. The methanol is removed under reduced pressure, AcOEt is added and the solution is washed with saturated, aqueous ammonium chloride and brine. The organic portion is dried over MgSO4, filtered, and concentrated under reduced pressure to yield 6.8 g (62%) of the title compound as a white solid. GCMS m/e 187 [M−H]−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08101761B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-90478131fd2643e281544e934bd8959d |
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| Source note | uspto-grants-2012_01 |
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