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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 33541Generated: October 28, 2026

Sodium borohydride → (5-(3-Chlorophenyl)pyridin-3-yl)methanol

https://huagongshe.com/reaction/33541

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantMethyl 5-(3-chlorophenyl)nicotinateHCID 20099850—
SolventEthanolHCID 702—
Product(5-(3-Chlorophenyl)pyridin-3-yl)methanolHCID 2472984629.4%

Reaction Conditions

Temperature50 °C

Reaction Steps

A solution of 1.0 g (4.04 mmol) 5-(3-Chloro-phenyl)-nicotinic acid methyl ester in 60.0 ml Ethanol was treated at room temperature (r. t.) with 304 mg (80.7 mmol) of sodium borohydride. The mixture was stirred over night at 50° C. Then it was poured on ice and extracted tree times with ethyl acetate. The combined organic phases were washed with water, dried (sodium sulphate) and evaporated. Chromatography on silica (eluent: ethyl acetate/n-heptane 1:1) gave 261 mg (26%) of [5-(3-Chloro-phenyl)-pyridin-3-yl]-methanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07429605B2
Source datasetuspto-grants-2008_09
ORD IDord-f2455bc280594cd2a7a7ddd2238e694e
Source noteuspto-grants-2008_09