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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Ethyl 4-chlorobenzoate | HCID 81785 | — |
| Edukt | Sodium ethoxide | HCID 2723922 | — |
| Edukt | 2-Amino-3-(2-quinolon-3-yl)propionic acid | HCID 13342097 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | 2-(4-Chlorobenzoylamino)-3-(2-quinolon-3-yl)propionic acid | HCID 13342103 | 9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04578381 |
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| Quelldatensatz | uspto-grants-1986_03 |
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| ORD ID | ord-aa6fb9ed376f4ebcb8a81c60ad956e85 |
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| Quellennotiz | uspto-grants-1986_03 |
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