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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1700114Erstellt: 27. Oktober 2026

Phenol → 2-Methyl-4-phenoxy-8-bromo-quinoline

https://huagongshe.com/reaction/1700114

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhenolHCID 996—
EduktPotassium HydroxideHCID 14797—
Edukt8-Bromo-4-chloro-2-methylquinolineHCID 768483—
LösungsmittelDichloromethaneHCID 6344—
Produkt2-Methyl-4-phenoxy-8-bromo-quinolineHCID 1831781584,9%

Reaktionsbedingungen

Temperatur120 °C

Reaktionsschritte

Part B: A mixture of 5.0 g (19.5 mmol) of 2-methyl-4-chloro-8-bromo-quinoline, 18.3 g (195 mmol) of phenol and 2.5 g (87%, 39 mmol) of KOH was heated at 120° C. under nitrogen for 30 min. After cooling 500 ml of CH2Cl2 was added and the mixture was extracted with 250 ml of 1N NaOH. After concentration of the organic layer in vacuo the residue was dissolved in ether and again extracted with 50 ml of 1N NaOH and 50 ml of brine. The organic layer was dried over magnesium sulphate and concentrated in vacuo. A total of 5.2 g of 2-methyl-4-phenoxy-8-bromo-quinoline was obtained as a white solid (85% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06350750B1
Quelldatensatzuspto-grants-2002_02
ORD IDord-42e6c802722443f5884c5a1eaf0fd463
Quellennotizuspto-grants-2002_02