HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 336864Erstellt: 24. Oktober 2026
Hydrochloric Acid → Ethyl 6-chloro-4-hydroxy-3-quinolinecarboxylate
https://huagongshe.com/de/reaction/336864
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | 4-Chloroaniline | HCID 7812 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | 3-Ethoxy-2-ethoxycarbonylprop-2-enoate | HCID 85829211 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | Ethyl 6-chloro-4-hydroxy-3-quinolinecarboxylate | HCID 718113 | 71% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08889706B2 |
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| Quelldatensatz | uspto-grants-2014_11 |
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| ORD ID | ord-e6dd59b80fae4a7cafa0105fa0fca600 |
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| Quellennotiz | uspto-grants-2014_11 |
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