Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1296998Generated: October 26, 2026

(o-Chlorophenyl)acetonitrile → 2-Biphenylacetonitrile

https://huagongshe.com/reaction/1296998

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(o-Chlorophenyl)acetonitrileHCID 76112—
ReactantPotassium FluorideHCID 522689—
ReactantHCID 178419127HCID 178419127—
Catalystpalladium(II) acetateHCID 167845—
Catalyst2-(Di-tert-butylphosphino)biphenylHCID 2734215—
SolventTetrahydrofuranHCID 8028—
Product2-BiphenylacetonitrileHCID 33410192.1%

Reaction Steps

An oven dried resealable Schlenk tube was evacuated and backfilled with argon and charged with palladium acetate (2.2 mg, 0.01 mmol, 1.0 mol %), 2-(di-tert-butylphosphino)biphenyl (6.0 mg, 0.020 mmol, 2.0 mol %), phenylboron dihydroxide (183 mg, 1.5 mmol), and potassium fluoride (174 mg, 3.0 mmol). The tube was evacuated and backfilled with argon, and THF (1 mL) and 2-chlorobenzyl cyanide (152 mg, 1.0 mmol) were added through a rubber septum. The tube was sealed with a teflon screwcap, and the reaction mixture was stirred at room temperature until the starting aryl chloride had been completely consumed as judged by GC analysis. The reaction mixture was then diluted with ether (30 mL) and poured into a separatory funnel. The mixture was washed with 1.0 M NaOH (20 mL), and the aqueous layer was extracted with ether (20 mL). The combined organic layers were washed with brine (20 mL), dried over anhydrous magnesium sulfate, filtered, and concentrated. The crude material was purified by flash chromatography on silica gel to afford 178 mg (92%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07247731B2
Source datasetuspto-grants-2007_07
ORD IDord-9ca75c6ad2cd41fbb5e1b42ddbf78350
Source noteuspto-grants-2007_07