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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 736379Generated: October 25, 2026

Potassium Carbonate → 5-Methyl-2-phenylpyridine

https://huagongshe.com/reaction/736379

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantPhenylboronic AcidHCID 66827—
Reactant2-Bromo-5-methylpyridineHCID 564216—
CatalystHCID 178418397HCID 178418397—
SolventAcetonitrileHCID 6342—
Product5-Methyl-2-phenylpyridineHCID 47467—

Reaction Steps

Phenylboronic acid (732 mg, 6 mmol), 2-bromo-5-methylpyridine (1.03 g, 5.99 mmol), and Pd (PPh3)4 (350 mg, 0.303 mmol) were heated in 0.4 M K2CO3 (30 mL, 12 mmol) and CH3CN (30 mL) at 90° overnight. The mixture was then cooled to room temperature and concentrated under reduced pressure. The residue was partitioned between brine and ethyl acetate. The organic layer was separated, dried (Na2SO4), filtered, and the filtrate was concentrated under reduced pressure. The residue was purified by column chromatography on silica gel (9:1 hexanes:ethyl acetate) to provide the title compound. 1H NMR (300 MHz, DMSO-d6) δ 8.50 (m, 1H), 8.05 (m, 2H), 7.85 (d, J=8.4 Hz, 1H), 7.68-7.71 (m, 1H), 7.37-7.50 (m, 3H), 2.34 (s, 3H); MS (APCI+) m/z 170 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07595332B2
Source datasetuspto-grants-2009_09
ORD IDord-9e7489330df747f0a94e6c7b2828f6bb
Source noteuspto-grants-2009_09