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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 431842Generated: October 31, 2026

2-Bromopyridine → 2-(4-Vinylphenyl)pyridine

https://huagongshe.com/reaction/431842

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromopyridineHCID 7973—
ReactantTetrahydrofuranHCID 8028—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Formylphenylboronic AcidHCID 591073—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
Product2-(4-Vinylphenyl)pyridineHCID 1171528980%

Reaction Conditions

Temperature90 °C

Reaction Steps

4-Formylphenylboronic acid (10.14 g, 0.0676 mol), 2-bromopyridine (12.64 g, 0.08 mol), tetrahydrofuran (100 ml), 2M potassium carbonate aqueous solution (26 ml), and palladium acetate (Pd(OAc)2, 0.04 g, 1 mol %) were placed into 250 ml of 2-necked round-bottomed flask under N2. The reaction mixture was refluxed at 90° C. for 24 hr and then poured in 200 ml of water in beaker. The reaction mixture was extracted with ether (3×150 ml) and the ether layer was then dried over magnesium sulfate (10 g) by stirring for 30 min. The dried ether layer was evaporated in vacuo to dryness and purified further by column chromatography on silica gel with eluting hexane/ethylacetate (1/5) to yield 2-(4-vinyl-phenyl)pyridine (80%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06660821B2
Source datasetuspto-grants-2003_12
ORD IDord-c86faa2f25644721a3f27faa45d993a0
Source noteuspto-grants-2003_12