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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1618664Generated: October 31, 2026

2,4-Dichloro-5,7-difluoro-3-methylquinoline → 3-((4-Chloro-5,7-difluoro-3-methylquinolin-2-yl)methyl)benzonitrile

https://huagongshe.com/reaction/1618664

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-Dichloro-5,7-difluoro-3-methylquinolineHCID 59631040—
ReactantHCID 178509756HCID 178509756—
CatalystHCID 178418397HCID 178418397—
SolventTetrahydrofuranHCID 8028—
Product3-((4-Chloro-5,7-difluoro-3-methylquinolin-2-yl)methyl)benzonitrileHCID 67285422—

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-cyanobenzyl)zinc(II) bromide (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 3-((4-chloro-5,7-difluoro-3-methylquinolin-2-yl)methyl)benzonitrile. Mass Spectrum (ESI) m/e=329.0 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765940B2
Source datasetuspto-grants-2014_07
ORD IDord-8cf4396bdee742e890061360a16698de
Source noteuspto-grants-2014_07