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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 33528Generated: October 26, 2026

Sodium borohydride → (5-(4-(Trifluoromethoxy)phenyl)pyridin-3-yl)methanol

https://huagongshe.com/reaction/33528

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant5-(4-Trifluoromethoxy-phenyl)-nicotinic acid methyl esterHCID 58002591—
SolventEthanolHCID 702—
Product(5-(4-(Trifluoromethoxy)phenyl)pyridin-3-yl)methanolHCID 2472984733.6%

Reaction Steps

A solution of 535 mg (1.76 mmol) 5-(4-Trifluoromethoxy-phenyl)-nicotinic acid methyl ester in 16 ml Ethanol was treated at room temperature (r. t.) with 67 mg (1.76 mmol) of sodium borohydride. The mixture was stirred for 4 h. at r. t., then two days at 80° C. The mixture 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/methanol 5:1) gave 159 mg (33%) of [5-(4-Trifluoromethoxy-phenyl)-pyridin-3-yl]-methanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07429605B2
Source datasetuspto-grants-2008_09
ORD IDord-d96599b542d2457c84ac0aa46c7c899b
Source noteuspto-grants-2008_09