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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1669296Generated: October 30, 2026

Sodium borohydride → HCID 59729434, compound

https://huagongshe.com/reaction/1669296

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 59729415HCID 59729415—
SolventEthanolHCID 702—
ProductHCID 59729434HCID 5972943483.3%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07989457B2
Source datasetuspto-grants-2011_08
ORD IDord-baa354baf8224db4a0412d04f9b0d649
Source noteuspto-grants-2011_08