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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1595255Generated: November 1, 2026

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

https://huagongshe.com/reaction/1595255

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 numberUS06288092B1
Source datasetuspto-grants-2001_09
ORD IDord-1271b06bb0894d8488ee6781e825921f
Source noteuspto-grants-2001_09