HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 571693Generated: October 31, 2026
Sodium borohydride → 2-Cyano-5-hydroxymethylpyridine
https://huagongshe.com/reaction/571693
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 5-Formylpyridine-2-carbonitrile | HCID 10986263 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-Cyano-5-hydroxymethylpyridine | HCID 12251966 | 86.6% |
Reaction Steps
To a 0° C. solution of 5-formylpicolinonitrile (490 mg, 3.71 mmol) in 15 mL of MeOH was added NaBH4 (140 mg, 3.71 mmol). The reaction mixture was stirred at 0° C. for 1 h and quenched with 5% citric acid. After most MeOH was removed by concentration, the residue was partitioned between DCM and sat. NaHCO3 (aq.). The aqueous layer was extracted with DCM (10×). The organic layer was washed with brine and dried (Na2SO4). The product 5-(hydroxymethyl)picolinonitrile (431 mg) was obtained by concentration under vacuum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09029362B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-798301b99eac48ad837b69b0a2095869 |
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| Source note | uspto-grants-2015_05 |
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