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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 228590Erstellt: 26. Oktober 2026

5-Bromo-2-hydroxybenzophenone → {5-Bromo-2-[(6,7-dimethoxy-4-quinolyl)oxy]phenyl}-(phenyl)methanone

https://huagongshe.com/reaction/228590

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt5-Bromo-2-hydroxybenzophenoneHCID 229009—
Edukt4-Chloro-6,7-dimethoxyquinolineHCID 459610—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
Lösungsmittel1,2-DichlorobenzeneHCID 7239—
Produkt{5-Bromo-2-[(6,7-dimethoxy-4-quinolyl)oxy]phenyl}-(phenyl)methanoneHCID 2487921094,5%

Reaktionsbedingungen

Temperatur160 °C

Reaktionsschritte

4-Chloro-6,7-dimethoxyquinoline (56.1 mg), 5-bromo-2-hydroxybenzophenone (361 mg), and 4-dimethylaminopyridine (168 mg) were suspended in o-dichlorobenzene (5 ml), and the suspension was stirred at 160° C. for 7 hr. The reaction solution was cooled to room temperature, and the solvent was then removed therefrom by distillation under the reduced pressure. Chloroform was added to the residue, and mixture was washed with a 1 N aqueous potassium hydroxide solution and saturated brine and was dried over anhydrous magnesium sulfate. The solvent was removed therefrom by distillation under the reduced pressure, and the residue was purified by column chromatography using chloroform and by thin layer chromatography using acetone-hexane to give the title compound (110 mg, yield 94%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07560558B2
Quelldatensatzuspto-grants-2009_07
ORD IDord-6f3beb0d05994b94832df27083e012ea
Quellennotizuspto-grants-2009_07