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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1354955Generated: October 27, 2026

3-Chloropyridine → 3-(3-Acetylphenyl)pyridine

https://huagongshe.com/reaction/1354955

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-ChloropyridineHCID 12287—
ReactantPotassium FluorideHCID 522689—
Reactant3-Acetylphenylboronic acidHCID 2734310—
Catalystpalladium(II) acetateHCID 167845—
Catalyst2-(Di-tert-butylphosphino)biphenylHCID 2734215—
SolventTetrahydrofuranHCID 8028—
Product3-(3-Acetylphenyl)pyridineHCID 1204072592%

Reaction Conditions

Temperature50 °C

Reaction Steps

An oven dried resealable Schlenk tube was evacuated and backfilled with argon and charged with palladium acetate (2.2 mg, 0.01 mmol, 1.0 mol %), 2-(di-tert-butylphosphino)biphenyl (6.0 mg, 0.020 mmol, 2.0 mol %), 3-acetylphenylboronic acid (246 mg, 1.5 mmol), and potassium fluoride (173 mg, 3.0 mmol). The tube was evacuated and backfilled with argon, and THF (1 mL) and 3-chloropyridine (0.095 mL, 1.0 mmol) were added through a rubber septum. The tube was sealed with a teflon screwcap, and the reaction mixture was heated to 50° C. with stirring until the starting aryl chloride had been completely consumed as judged by GC analysis. The reaction mixture was then diluted with ether (30 mL) and poured into a separatory funnel. The mixture was washed with water (20 mL), and the aqueous layer was extracted with ether (20 mL). The combined organic layers were washed with brine (20 mL), dried over anhydrous magnesium sulfate, filtered, and concentrated. The crude material was purified by flash chromatography on silica gel to afford 181 mg (92%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07223879B2
Source datasetuspto-grants-2007_05
ORD IDord-a1bb6698fca7411d90d21111077778e1
Source noteuspto-grants-2007_05