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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 228687Erstellt: 27. Oktober 2026

4-Chloro-6,7-dimethoxyquinoline → 4-(2-Iodo-4,5-dimethyl-phenoxy)-6,7-dimethoxyquinoline

https://huagongshe.com/reaction/228687

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Chloro-6,7-dimethoxyquinolineHCID 459610—
Edukt2-Iodo-4,5-dimethylphenolHCID 13635257—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
Lösungsmittel1,2-DichlorobenzeneHCID 7239—
Produkt4-(2-Iodo-4,5-dimethyl-phenoxy)-6,7-dimethoxyquinolineHCID 2307836157,6%

Reaktionsbedingungen

Temperatur130 °C

Reaktionsschritte

2-Iodo-4,5-dimethylphenol (447 mg), 4-chloro-6,7-dimethoxyquinoline (466 mg), and 4-dimethylaminopyridine (539 mg) were suspended in o-dichlorobenzene (20 ml), and the mixture was stirred at 130° C. for 4 hr. The reaction solution was cooled to room temperature, and the solvent was then 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 by distillation under the reduced pressure. The residue was purified by column chromatography using acetone-chloroform to give the title compound (452 mg, yield 50%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07560558B2
Quelldatensatzuspto-grants-2009_07
ORD IDord-375447432ad448ada733883bacae3148
Quellennotizuspto-grants-2009_07