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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1010079Erstellt: 25. Oktober 2026

Ethanol → 4-(4-Aminophenoxy)-6-cyano-7-(2-methoxyethoxy)quinoline

https://huagongshe.com/reaction/1010079

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolHCID 702—
EduktAmmonium ChlorideHCID 25517—
Edukt6-Cyano-7-(2-methoxyethoxy)-4-(4-nitrophenoxy)quinolineHCID 22936341—
KatalysatorIronHCID 23925—
LösungsmittelWaterHCID 962—
Produkt4-(4-Aminophenoxy)-6-cyano-7-(2-methoxyethoxy)quinolineHCID 2293650672,6%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

6-Cyano-7-(2-methoxyethoxy)-4-(4-nitrophenoxy)quinoline (1.8 g), iron (1.8 g) and ammonium chloride (3.6 g) were suspended in an ethanol (30 ml)-water (7 ml) mixed solvent and the suspension was heated and stirred at 80° C. for 2 hours. After completion of the reaction, the reaction mixture was filtered with celite and washed in ethyl acetate. The organic layer was washed with saturated brine, dried over magnesium sulfate and concentrated. The obtained solid was washed with ether and dried to obtain 1.2 g of the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07973160B2
Quelldatensatzuspto-grants-2011_07
ORD IDord-4472f3fd17db4f5d8898f0db62e71a5d
Quellennotizuspto-grants-2011_07