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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1412255Generated: October 31, 2026

Toluene → 2'-Fluoro-4'-(hydroxymethyl)biphenyl-2-carbonitrile

https://huagongshe.com/reaction/1412255

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantSodium CarbonateHCID 10340—
Reactant2-Cyanophenylboronic acidHCID 2734610—
Reactant2-Fluoro-4-formylbenzeneboronic acidHCID 16218045—
CatalystTetrabutylammonium BromideHCID 74236—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventEthyl AcetateHCID 8857—
Product2'-Fluoro-4'-(hydroxymethyl)biphenyl-2-carbonitrileHCID 6700999030%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of (2-fluoro-4-formylphenyl)boronic acid (35.3 g), 2-cyano-phenylboronic acid (40.0 g), [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium (1.7 g), tetrabutylammonium bromide (0.68 g), 2M aqueous sodium carbonate solution (200 mL) and toluene (600 mL) was stirred at 100° C. for 72 hr under an argon atmosphere. The reaction mixture was diluted with ethyl acetate, washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure. The obtained residue was dissolved in tetrahydrofuran (150 mL) and methanol (150 mL), sodium borohydride (8.7 g) was added, 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 (14.1 g, 30%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921379B2
Source datasetuspto-grants-2014_12
ORD IDord-8cbd521d8db74ed7a6a80781d3a3d4c9
Source noteuspto-grants-2014_12