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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1885532Generated: November 1, 2026

4,7-Dichloroquinoline → 7-Chloro-4-[(4-fluorophenyl)methyl]quinoline

https://huagongshe.com/reaction/1885532

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4,7-DichloroquinolineHCID 6866—
ReactantSodium amideHCID 24533—
ReactantBenzeneacetonitrile, 4-fluoro-HCID 68016—
SolventBenzeneHCID 241—
Solvent1-ButanolHCID 263—
SolventHydrochloric AcidHCID 313—
Product7-Chloro-4-[(4-fluorophenyl)methyl]quinolineHCID 16417567%

Reaction Steps

A solution of 100 g (740 mmol) of 4-fluorophenylacetonitrile in 200 ml of benzene was added to a cooled (0° C.) slurry of 40 g (945 mmol) of sodium amide in 600 ml of the same solvent. After the addition was complete the solution was warmed to ambient temperature and stirred for one-half hour. The reaction mixture was again cooled to 0° C., 73.2 g (370 mmol) of solid 4,7-dichloroquinoline was added in increments, and the mixture was then stirred at ambient temperature overnight. Quenching with NH4Cl followed by workup gave the crude disubstituted acetonitrile, which was dissolved in 500 ml of n-butanol saturated with anhydrous HCl. The acidic solution was heated at reflux for 18 hours. The majority of the solvent was removed via distillation, and the residue was diluted with solvent, and washed with 10% NaOH. The organic layer was dried, and the solvent was removed in vacuo. Purification via HPLC gave 67 g of the title product. Yield: 67%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05145843
Source datasetuspto-grants-1992_09
ORD IDord-99ff8803823d455bafeacac8adfeb048
Source noteuspto-grants-1992_09