HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 231980Generated: October 30, 2026
Potassium Iodide → Acetonitrile, [(5,7-dichloro-2-methyl-8-quinolinyl)oxy]-
https://huagongshe.com/reaction/231980
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Chlorquinaldol | HCID 6301 | — |
| Reactant | Chloroacetonitrile | HCID 7856 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | Acetonitrile, [(5,7-dichloro-2-methyl-8-quinolinyl)oxy]- | HCID 2681672 | — |
Reaction Steps
10.7 g of 5,7-dichloro-8-hydroxyquinaldine are dissolved at elevated temperature in 150 ml of 2-butanone; 10.4 g of potassium carbonate are then added portionwise, and the mixture is refluxed for one hour. After the addition of 1 g of potassium iodide, there are added dropwise, with stirring and refluxing, 7.1 g of chloroacetonitrile in 30 ml of 2-butanone, and the mixture is subsequently heated for 3 hours at an internal temperature of 75° C. To the resulting reaction mixture, after cooling to room temperature, is added 1 liter of water, and the whole is filtered; the residue is washed with water, dried, and recrystallised from chloroform/petroleum ether (40°-60° C.) to thus obtain 2-methyl-5,7-dichloro-8-(cyanomethoxy)-quinoline, m.p. 157°-158° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04851033 |
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| Source dataset | uspto-grants-1989_07 |
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| ORD ID | ord-b1e67ff4e1c3449fad188a617935bea5 |
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| Source note | uspto-grants-1989_07 |
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