HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1669296Generated: October 30, 2026
Sodium borohydride → HCID 59729434, compound
https://huagongshe.com/reaction/1669296
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 59729415 | HCID 59729415 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 59729434 | HCID 59729434 | 83.3% |
Reaction Steps
2-(6-Chloro-pyridin-3-yl)-octanal (1.02 g, 4.26 mmol) is dissolved into denatured ethanol (20 mL) at room temperature then cooled to 0° C. in an ice bath. Sodium borohydride (0.162 g, 4.26 mmol) is then carefully added in small portions. The reaction is allowed to warm slowly to room temperature and is monitored by HPLC. Upon complete consumption of starting material, the reaction is carefully quenched with water and diluted with ethyl acetate. The ethanol is removed and the residue is extracted with ethyl acetate, washed, dried, and concentrated. The 2-(6-Chloro-pyridin-3-yl)-octan-1-ol (0.856 g, 3.55 mmol), 83%, is obtained in purified form after flash column chromatography.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07989457B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-baa354baf8224db4a0412d04f9b0d649 |
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| Source note | uspto-grants-2011_08 |
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