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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2048239Generated: October 30, 2026

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

https://huagongshe.com/reaction/2048239

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 numberUS08592431B2
Source datasetuspto-grants-2013_11
ORD IDord-9bd5071cbbf34012879a187dc1275001
Source noteuspto-grants-2013_11