Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1700115Erstellt: 25. Oktober 2026

Water → 2-Methyl-4-phenoxy-8-(2,4,6-trimethylphenyl)-quinoline

https://huagongshe.com/reaction/1700115

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
Edukt2,4,6-Trimethylbenzeneboronic acidHCID 292184—
Edukt2-Methyl-4-phenoxy-8-bromo-quinolineHCID 18317815—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelWater 1,2-dimethoxyethaneHCID 18180031—
Produkt2-Methyl-4-phenoxy-8-(2,4,6-trimethylphenyl)-quinolineHCID 1831781673%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

Part C: To a solution of 5.2 g (16.5 mmol) of 2-methyl-4-phenoxy-8-bromo-quinoline in 175 ml DME-water (6:1), 3.3 g (20 mmol) of 2,4,6-tri-methyl-phenyl-boronic acid, 12.6 g (40 mmol) of Ba(OH)2.8H2O and 0.46 g (0.4 mmol) of tetrakis(triphenylphosphine)palladium were added. After heating at 80° C. for 16 hours the mixture was cooled to room temperature, water was added and the mixture was extracted with CH2Cl2. The organic layer was dried over magnesium sulphate and concentrated in vacuo. The product was purified on a silicagel column using CH2Cl2 as the eluent. A total of 4.2 g of 2-methyl-4-phenoxy-8-(2,4,6-trimethylphenyl)-quinoline was obtained (73% yield)

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06350750B1
Quelldatensatzuspto-grants-2002_02
ORD IDord-b35a9f33effd4194a0f6070a95547eee
Quellennotizuspto-grants-2002_02