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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 483178Erstellt: 24. Oktober 2026

Ethyl 4-chlorobenzoate → 2-(4-Chlorobenzoylamino)-3-(2-quinolon-3-yl)propionic acid

https://huagongshe.com/de/reaction/483178

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl 4-chlorobenzoateHCID 81785—
EduktSodium ethoxideHCID 2723922—
Edukt2-Amino-3-(2-quinolon-3-yl)propionic acidHCID 13342097—
LösungsmittelEthanolHCID 702—
Produkt2-(4-Chlorobenzoylamino)-3-(2-quinolon-3-yl)propionic acidHCID 133421039%

Reaktionsschritte

In 100 ml of ethanol, 1.66 g of ethyl p-chlorobenzate, 0.5 g of sodium ethylate and 2.09 g of 2-amino-3-(2-quinolon-3-yl)propionic acid were added and the whole mixture was placed in an autoclave. The reaction was carried out under 110 atmospheric pressure at 140°-150° C. for 6 hours. After completion of the reaction, the reaction mixture was cooled and concentrated under a reduced pressure. The residue was dissolved in 200 ml of chloroform, washed with 1%-potassium carbonate aqueous solution, a diluted hydrochloric acid and water in this order, then the chloroform layer was dried with sodium sulfate. The solvent was removed by distillation, the residue was recrystallized from ethanol-water to obtain 300 mg of 2-(4-chlorobenzoylamino)-3-(2-quinolon-3-yl)propionic acid in the form of white powdery product.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04578381
Quelldatensatzuspto-grants-1986_03
ORD IDord-aa6fb9ed376f4ebcb8a81c60ad956e85
Quellennotizuspto-grants-1986_03