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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2062434Generated: November 1, 2026

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

https://huagongshe.com/reaction/2062434

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 numberUS08283353B2
Source datasetuspto-grants-2012_10
ORD IDord-cb5dc1b468ac43e7bc792f33f7c333aa
Source noteuspto-grants-2012_10