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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5544Generated: October 25, 2026

4,7-Dichloroquinoline → 7-Chloro-4-(4-fluorophenoxy)quinoline

https://huagongshe.com/reaction/5544

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4,7-DichloroquinolineHCID 6866—
Reactant4-FluorophenolHCID 9732—
Reactant4-PyrrolidinopyridineHCID 75567—
SolventO-XyleneHCID 7237—
Product7-Chloro-4-(4-fluorophenoxy)quinolineHCID 164171649.9%

Reaction Steps

To a 50 mL flask equipped with a condenser, drying tube and thermometer, was added 1.98 g (0.01 moles) of 4,7-dichloroquinoline, 1.57 g (0.0014 moles) of 4-fluorophenol, 0.22 g (0.0015 moles) of 4-pyrrolidinopyridine and 20 mL of xylene. The reaction mixture was heated to reflux and reaction progress was monitored by TLC. After 18 hr, the mixture was cooled and washed with 50 mL of 5 N NaOH. The caustic layer was extracted with 3×20 mL of diethyl ether. The xylene and the ether layers were combined and dried over Na2SO4. Removal of the solvent provided 2.49 g (91 percent yield) of product, mp=88°-91° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05245036
Source datasetuspto-grants-1993_09
ORD IDord-083e912021ea4636b30489d9253b9684
Source noteuspto-grants-1993_09