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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4,7-Dichloroquinoline | HCID 6866 | — |
| Reactant | Sodium amide | HCID 24533 | — |
| Reactant | Benzeneacetonitrile, 4-fluoro- | HCID 68016 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | 7-Chloro-4-[(4-fluorophenyl)methyl]quinoline | HCID 164175 | 67% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05145843 |
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| Source dataset | uspto-grants-1992_09 |
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| ORD ID | ord-99ff8803823d455bafeacac8adfeb048 |
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| Source note | uspto-grants-1992_09 |
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