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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 922808Generated: October 31, 2026

Toluene → 7-Chloro-4-(2-fluoro-4-methoxyphenyl)quinoline-2-carbonitrile

https://huagongshe.com/reaction/922808

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantSodium CarbonateHCID 10340—
Reactant(2-Fluoro-4-methoxyphenyl)boronic acidHCID 15789384—
Reactant4,7-Dichloroquinoline-2-carbonitrileHCID 57437829—
CatalystHCID 178418397HCID 178418397—
SolventEthyl AcetateHCID 8857—
Product7-Chloro-4-(2-fluoro-4-methoxyphenyl)quinoline-2-carbonitrileHCID 8954358452.3%

Reaction Conditions

Temperature75 °C

Reaction Steps

To a stirred solution of 4,7-dichloroquinoline-2-carbonitrile (6 g, 26.9 mmol), (2-fluoro-4-methoxyphenyl)boronic acid (5.03 g, 29.6 mmol), 2M sodium carbonate (29.6 ml, 59.2 mmol) in 10:1 toluene (48.9 ml) ethanol (4.89 ml) was added tetrakis(triphenylphosphine)palladium(0) (0.777 g, 0.672 mmol). The mixture was stirred at 75° C. under N2 for 18 hours. The reaction was allowed to cool to ambient temperature. The cooled reaction mixture was diluted with EtOAc and then washed with H2O, brine, dried (MgSO4) and concentrated. The residue was mostly dissolved in warm EtOAc (100 ml), added 100 ml of Et2O, allowed to stand at ambient temperature for 1 hour. The solid was collected and washed with cold Et2O (50 ml) to give 7-chloro-4-(2-fluoro-4-methoxyphenyl)quinoline-2-carbonitrile (4.4 g, 14.07 mmol, 52.3% yield) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09278960B2
Source datasetuspto-grants-2016_03
ORD IDord-043c0f46d0a242ee9fa78391287e62b8
Source noteuspto-grants-2016_03