HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 228571Erstellt: 24. Oktober 2026
Water → 2-[(6,7-Dimethoxy-4-quinolyl)oxy]-5-trifluoromethoxybenzaldehyde
https://huagongshe.com/de/reaction/228571
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | 4-Chloro-6,7-dimethoxyquinoline | HCID 459610 | — |
| Edukt | 2-Hydroxy-5-(trifluoromethoxy)benzaldehyde | HCID 1268058 | — |
| Katalysator | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Lösungsmittel | Chlorobenzene | HCID 7964 | — |
| Produkt | 2-[(6,7-Dimethoxy-4-quinolyl)oxy]-5-trifluoromethoxybenzaldehyde | HCID 23078303 | — |
Reaktionsschritte
4-Chloro-6,7-dimethoxyquinoline (111 mg), 5-trifluoromethoxysalicylaldehyde (412 mg), and 4-dimethylaminopyridine (244 mg) were suspended in monochlorobenzene (2 ml), and the suspension was stirred at 130° C. overnight. 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 chromatography on silica gel using ethyl acetate-hexane for development to give 2-[(6,7-dimethoxy-4-quinolyl)oxy]-5-trifluoromethoxybenzaldehyde.
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-cd988899331d4b8587f8382755d24441 |
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| Quellennotiz | uspto-grants-2009_07 |
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