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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 336866Erstellt: 24. Oktober 2026

Hydrochloric Acid → Ethyl 6-chloro-4-hydroxy-3-quinolinecarboxylate

https://huagongshe.com/de/reaction/336866

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
Edukt4-ChloroanilineHCID 7812—
EduktSodium HydroxideHCID 14798—
Edukt3-Ethoxy-2-ethoxycarbonylprop-2-enoateHCID 85829211—
LösungsmittelWaterHCID 962—
LösungsmittelEthyl AcetateHCID 8857—
ProduktEthyl 6-chloro-4-hydroxy-3-quinolinecarboxylateHCID 71811371%

Reaktionsschritte

A mixture of 4-chloroaniline (156.7 mmol) and ethyl ethoxymethylenemalonate (156.7 mmol) was stirred at room temperature until homogeneous. The homogeneous solution was heated in an oil bath at 165° C. for 6 hours. The reaction mixture was cooled to room temperature and 1 N HCl (3 mL) was added. The reaction mixture was stirred and heated to 115° C. for 3 hours. The mixture was cooled to room temperature and then treated with 20 mL of water. The resulting suspension treated with 10 N NaOH solutions to reach the pH about 8. It was partitioned between ethyl acetate and water. The organic layer was separated and the aqueous layer was extracted with ethyl acetate. The combined organic extracts were washed with brine, dried over MgSO4, filtered and concentrated. The crude product was purified by flash column chromatography using a 9:1 v/v hexane:ethyl acetate as solvent to afford title compound (28 g, 71% yield) as a yellow solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08889706B2
Quelldatensatzuspto-grants-2014_11
ORD IDord-28e71f7ff3ed46ceb3c9424e15ce4dbf
Quellennotizuspto-grants-2014_11