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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 228548Erstellt: 24. Oktober 2026

Xanthoxylin → 1-{4,6-Dimethoxy-2-[(6,7-dimethoxy-4-quinolyl)oxy]-phenyl}-1-ethanone

https://huagongshe.com/de/reaction/228548

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktXanthoxylinHCID 66654—
Edukt4-Chloro-6,7-dimethoxyquinolineHCID 459610—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
Lösungsmittel1,2-DichlorobenzeneHCID 7239—
Produkt1-{4,6-Dimethoxy-2-[(6,7-dimethoxy-4-quinolyl)oxy]-phenyl}-1-ethanoneHCID 5775636527%

Reaktionsbedingungen

Temperatur120 °C

Reaktionsschritte

4-Chloro-6,7-dimethoxyquinoline (56 mg), 2-hydroxy-4,6-dimethoxyacetophenone (196 mg), and 4-dimethylaminopyridine (122 mg) were suspended in o-dichlorobenzene (1 ml), and the suspension was stirred at 120° C. overnight. The reaction solution was cooled to room temperature, and the solvent was removed by distillation under the reduced pressure. Water was then added to the residue, and the mixture was extracted with chloroform. The chloroform layer was washed with water and was dried over anhydrous sodium sulfate. The solvent was removed therefrom by distillation under the reduced pressure. The residue was purified by column chromatography using acetone-hexane to give the title compound (25 mg, yield 27%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07560558B2
Quelldatensatzuspto-grants-2009_07
ORD IDord-2698dd9263034d84b4c14d37e94e58bd
Quellennotizuspto-grants-2009_07