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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1374841Generated: October 28, 2026

Acetonitrile → 2-Biphenylacetonitrile

https://huagongshe.com/reaction/1374841

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantPotassium CyanideHCID 9032—
Reactant18-Crown-6HCID 28557—
Reactant1-(Bromomethyl)-2-phenylbenzeneHCID 263365—
SolventWaterHCID 962—
Product2-BiphenylacetonitrileHCID 334101—

Reaction Steps

2-(Bromomethyl)biphenyl (1.35 g, 5.48 mmol), potassium cyanide (368 mg, 5.65 mmol), and a catalytic amount of 18-crown-6 ether were added to acetonitrile (10 ml), and the mixture was heated under reflux for 5 days. The reaction mixture was added with water and extracted with ethyl acetate. The extract was washed with saturated aqueous sodium bicarbonate solution and saturated brine, and dried over magnesium sulfate. Insoluble solids were removed by filtration, and the filtrate was concentrated under reduced pressure. The resulting oil was purified by silica gel column chromatography (ethyl acetate-hexane) to obtain the title compound as colorless solid (1.07 g, yield: quantitative).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07166617B2
Source datasetuspto-grants-2007_01
ORD IDord-4fb1bbc0107848d58f5e71a0d33626a6
Source noteuspto-grants-2007_01