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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1433343Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/1433343

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
PatentnummerUS07612092B2
Quelldatensatzuspto-grants-2009_11
ORD IDord-8493b43b9bf04d0fa208cf4201bd1b2f
Quellennotizuspto-grants-2009_11