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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2187517Generated: October 31, 2026

Sodium Carbonate → 4-[4-Methoxy-3-(phenyl)phenyl]pyridine

https://huagongshe.com/reaction/2187517

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant3-BromobenzonitrileHCID 23381—
ReactantTri-o-tolylphosphineHCID 80271—
Reactant[2-Methoxy-5-(pyridin-4-yl)phenyl]boronic acidHCID 18476091—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product4-[4-Methoxy-3-(phenyl)phenyl]pyridineHCID 9903337—

Reaction Conditions

Temperature80 °C

Reaction Steps

A stirred mixture of 3-bromobenzonitrile (0.91 g, 5.0 mmol), 2-Methoxy-5-(pyridin-4-yl)phenylboronic acid (0.50 g, 2.3 mmol), tri-o-tolylphosphine (0.152 g, 0.50 mmol), palladium (II) acetate (0.056 g, 0.25 mmol), sodium carbonate (1.59 g, 15 mmol) and water (15 mL) in dimethylformamide (46 mL) is heated at 80° C. for 5 h. The mixture is then treated with water (100 mL) and extracted with ethyl acetate (3×80 mL). The combined extracts are dried (Na2SO4), filtered and the solvent is evaporated off under reduced pressure to yield the crude product which is purified by chromatography (silica gel, ethyl acetate) to give 4-[4-methoxy-3-(phenyl)phenyl]pyridine base. The base is dissolved in diethylether (5 mL), treated with methanolic HCl (excess), evaporated to dryness under reduced pressure and recrystallised from ethanol-ether to give 4-[2-methoxy-3′-cyano-biphenyl-5-yl]pyridine, hydrochloride as a pale-yellow crystalline solid, m.p. 142-150° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06410547B1
Source datasetuspto-grants-2002_06
ORD IDord-3d730bd8e19749e6b02cb3efe81bf952
Source noteuspto-grants-2002_06