HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1449834Erstellt: 25. Oktober 2026
Diethyl Malonate → Ethyl 2-(3-chloro-2,4-difluorobenzoyl)-3-ethoxy-acrylate
https://huagongshe.com/reaction/1449834
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Diethyl Malonate | HCID 7761 | — |
| Edukt | 3-Chloro-2,4-difluorobenzoyl chloride | HCID 2773538 | — |
| Edukt | Diethyl (3-chloro-2,4-difluorobenzoyl)malonate | HCID 22077280 | — |
| Edukt | Ethyl (3-chloro-2,4-difluoro-benzoyl)-acetate | HCID 54232984 | — |
| Edukt | Ethyl orthoformate acetic anhydride | HCID 86583744 | — |
| Produkt | Ethyl 2-(3-chloro-2,4-difluorobenzoyl)-3-ethoxy-acrylate | HCID 54286793 | — |
Reaktionsschritte
Reaction of 3-chloro-2,4-difluoro-benzoyl chloride with diethyl malonate gives diethyl (3-chloro-2,4-difluoro-benzoyl)-malonate, and partial hydrolysis and decarboxylation lead to ethyl (3-chloro-2,4-difluoro-benzoyl)-acetate, which is reacted with ethyl orthoformate/acetic anhydride to give ethyl 2-(3-chloro-2,4-di-fluorobenzoyl)-3-ethoxy-acrylate; further reaction with cyclopropylamine leads to ethyl 2-(3-chloro-2,4-difluoro-benzoyl)-3-cyclopropylaminoacrylate, which is cyclized with potassium carbonate/dimethylformamide to give ethyl 8-chloro-1-cyclopropyl-7-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylate; hydrolysis then finally leads to the corresponding carboxylic acid. The reaction sequence described can be represented by the following equation: ##STR4##
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05599980 |
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| Quelldatensatz | uspto-grants-1997_02 |
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| ORD ID | ord-23bfccb877984dbf9f6bfe7d63307a61 |
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| Quellennotiz | uspto-grants-1997_02 |
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