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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2308153Generated: November 2, 2026

Potassium Carbonate → 4-Methyl-2-phenylquinoline

https://huagongshe.com/reaction/2308153

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantTriphenylphosphineHCID 11776—
ReactantPhenylboronic AcidHCID 66827—
Reactant2-Chloro-4-methylquinolineHCID 69449—
Catalystpalladium(II) acetateHCID 167845—
Solvent1,2-DimethoxyethaneHCID 8071—
SolventEthyl AcetateHCID 8857—
Product4-Methyl-2-phenylquinolineHCID 2091961%

Reaction Steps

2-Chloro-4-methylquinoline (5.0 g, 30 mmol) and phenyl boronic acid (4.4 g, 36 mmol) were dissolved into 100 mL of ethylene glycol dimethyl ether. To the stirred reaction was added triphenylphosphine (0.8 g) and palladium(II) acetate, followed by 50 mL of a 2 M solution of potassium carbonate. The reaction was refluxed for 16 hours. After cooling, the aqueous layer was discarded and additional ethyl acetate added. The organics were washed with a saturated solution of sodium chloride and separated. The organic layer was dried over magnesium sulfate, concentrated, and purified on a silica gel column using 20% ethyl acetate and hexanes as the eluants. The pure fractions were combined and concentrated to give 2-phenyl-4-methylquinoline (4.0 g, 61% yield) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06835469B2
Source datasetuspto-grants-2004_12
ORD IDord-e2cf8114536042a0951a2f81f871b771
Source noteuspto-grants-2004_12