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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1618660Generated: October 26, 2026

2,4-Dichloro-5,7-difluoro-3-methylquinoline → 4-Chloro-5,7-difluoro-2-(3-fluorobenzyl)-3-methylquinoline

https://huagongshe.com/reaction/1618660

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-Dichloro-5,7-difluoro-3-methylquinolineHCID 59631040—
ReactantHCID 178505699HCID 178505699—
CatalystHCID 178418397HCID 178418397—
SolventTetrahydrofuranHCID 8028—
Product4-Chloro-5,7-difluoro-2-(3-fluorobenzyl)-3-methylquinolineHCID 67284367—

Reaction Conditions

Temperature60 °C

Reaction Steps

A screw cap vial was charged with 2,4-dichloro-5,7-difluoro-3-methylquinoline (500 mg, 2.016 mmol), tetrakis(triphenylphosphine)palladium(0) (233 mg, 0.202 mmol), and THF (5.04 mL). The mixture was sparged with N2, then 3-fluoro-benzylzinc chloride (0.5M in THF, 4.23 mL, 2.116 mmol) was added and the reaction stirred at 60° C. for 2 h. The reaction was then partitioned between EtOAc and water, and the organic layer washed with brine, dried (MgSO4), and concentrated. The crude material was purified by flash chromatography, eluting with a gradient of 0-15% EtOAc in hexane to give 4-chloro-5,7-difluoro-2-(3-fluorobenzyl)-3-methylquinoline. Mass Spectrum (ESI) m/e=322.0 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765940B2
Source datasetuspto-grants-2014_07
ORD IDord-48e495a0e4d24589b1e8aaa4cbd2755d
Source noteuspto-grants-2014_07