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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1858014Generated: October 25, 2026

Benzene → 5-Phenylpyridine-2-carbonitrile

https://huagongshe.com/reaction/1858014

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantSodium CarbonateHCID 10340—
ReactantPhenylboronic AcidHCID 66827—
Reactant5-Bromopyridine-2-carbonitrileHCID 817154—
CatalystHCID 178420430HCID 178420430—
SolventEthanolHCID 702—
Product5-Phenylpyridine-2-carbonitrileHCID 935276136.7%

Reaction Steps

A mixture comprising 5-bromopyridine-2-carbonitrile (0.09 g, 0.49 mmol), phenyl boronic acid (0.12 g, 0.98 mmol), 2M sodium carbonate ((0.98 mL, 1.96 mmol), tetrakis(tritylphosphanyl)palladium (0.06 g, 0.049 mmol), benzene (2 mL) and ethanol (2 mL) was heated at reflux for 1 hour and then partitioned between ethyl acetate and water. The organic layer was separated, washed with water, dried (MgSO4) and concentrated. The residue was purified by silica gel chromatography (25% ethyl acetate/hexanes) to provide 5-phenylpyridine-2-carbonitrile (0.12 g, 0.67 mmol). MS (CI), Calculated for C12H8N2, 180.2, Found (MH+): 182.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06150379
Source datasetuspto-grants-2000_11
ORD IDord-96de982658ac4e01a4410be3ef68cd39
Source noteuspto-grants-2000_11