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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 519499Generated: October 31, 2026

Sodium borohydride → 4'-(Hydroxymethyl)-3'-(trifluoromethyl)biphenyl-2-carbonitrile

https://huagongshe.com/reaction/519499

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant4'-Formyl-3'-(trifluoromethyl)biphenyl-2-carbonitrileHCID 86644026—
SolventMethanolHCID 887—
Product4'-(Hydroxymethyl)-3'-(trifluoromethyl)biphenyl-2-carbonitrileHCID 6700985996.2%

Reaction Steps

To a solution (50 mL) of 4′-formyl-3′-(trifluoromethyl)biphenyl-2-carbonitrile (3.2 g) in methanol was added sodium borohydride (0.66 g), and the mixture was stirred at room temperature for 1 hr. After evaporation of the solvent under reduced pressure, the residue was extracted with water and ethyl acetate. The obtained ethyl acetate layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography to give the title compound as a colorless solid (3.1 g, 95%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115136B2
Source datasetuspto-grants-2015_08
ORD IDord-0a53a6172c56425bb6ce478432861d3e
Source noteuspto-grants-2015_08