HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 228527Erstellt: 24. Oktober 2026
Water → 4-[(1,6-Dibromo-2-naphthyl)oxy]-6,7-dimethoxyquinoline
https://huagongshe.com/de/reaction/228527
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | 2-Naphthol, 1,6-dibromo- | HCID 27768 | — |
| Edukt | 4-Chloro-6,7-dimethoxyquinoline | HCID 459610 | — |
| Katalysator | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Lösungsmittel | 1,2-Dichlorobenzene | HCID 7239 | — |
| Produkt | 4-[(1,6-Dibromo-2-naphthyl)oxy]-6,7-dimethoxyquinoline | HCID 68829718 | 67% |
Reaktionsschritte
4-Chloro-6,7-dimethoxyquinoline (223 mg), 1,6-dibromo-2-naphthol (910 mg), and 4-dimethylaminopyridine (366 mg) were suspended in o-dichlorobenzene (3 ml), and the suspension was stirred at 150° C. for 4 hr. The reaction solution was cooled to room temperature, water was then added to the reaction solution, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was then washed with water and saturated brine and was dried over anhydrous sodium sulfate. The solvent was removed therefrom by distillation under the reduced pressure, and the residue was purified by column chromatography using acetone-chloroform to give 4-[(1,6-dibromo-2-naphthyl)oxy]-6,7-dimethoxyquinoline (326 mg, yield 67%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07560558B2 |
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| Quelldatensatz | uspto-grants-2009_07 |
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| ORD ID | ord-1c329b09909a4651a0afb3a40c21d47c |
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| Quellennotiz | uspto-grants-2009_07 |
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