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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1618656Generated: October 28, 2026

Toluene → 4-Chloro-5,7-difluoro-3-methyl-2-(naphthalen-1-yl)quinoline

https://huagongshe.com/reaction/1618656

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantSodium CarbonateHCID 10340—
Reactant(Naphthalen-2-yl)boronic acidHCID 2734375—
Reactant2,4-Dichloro-5,7-difluoro-3-methylquinolineHCID 59631040—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
Product4-Chloro-5,7-difluoro-3-methyl-2-(naphthalen-1-yl)quinolineHCID 67284469—

Reaction Conditions

Temperature100 °C

Reaction Steps

A microwave vessel was charged with 2,4-dichloro-5,7-difluoro-3-methylquinoline (250 mg, 1.008 mmol), 2-naphthylboronic acid (225 mg, 1.310 mmol), tetrakis(triphenylphosphine)palladium(0) (87 mg, 0.076 mmol), sodium carbonate (534 mg, 5.04 mmol), toluene (8.06 mL), and water (2.02 mL). The mixture was heated at 100° C. for 2 h, then cooled to rt and partitioned between EtOAc and water. The organic layer was washed with brine, dried (MgSO4), and concentrated. The resulting crude material was purified by flash chromatography, eluting with a gradient of 0-6% EtOAc in hexane to give 4-chloro-5,7-difluoro-3-methyl-2-(naphthalen-1-yl)quinoline. Mass Spectrum (ESI) m/e=340.0 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765940B2
Source datasetuspto-grants-2014_07
ORD IDord-f1e8c2adad5d4874ab91156b28edb5c6
Source noteuspto-grants-2014_07