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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2255432Generated: November 2, 2026

4,7-Dichloroquinoline → HCID 19738138, compound

https://huagongshe.com/reaction/2255432

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4,7-DichloroquinolineHCID 6866—
Reactant4-FluoroanilineHCID 9731—
SolventEthyl AcetateHCID 8857—
ProductHCID 19738138HCID 1973813846.1%

Reaction Conditions

Temperature160 °C

Reaction Steps

To 2.0 g of 4,7-dichloroquinoline was added 2.24 g of 4-fluoroaniline, and the mixture was heated with stirring to 160° C. After a few minutes at this temperature, the mixture smoked and the melt solidified. The solid was allowed to cool and was then dissolved in ethyl acetate and washed to remove the aniline. The organic layer was dried over MgSO4 and then solvent was removed using reduced pressure. The residue was recrystallized in heptane to yield 1.27 g of 7-chloro-N-(4-fluorophenyl)-4-quinolinamine. M.P. 214°-16° C. (46.1% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05240940
Source datasetuspto-grants-1993_08
ORD IDord-35aa06d05517449d9d28015946ac6f6a
Source noteuspto-grants-1993_08