HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 24548Erstellt: 25. Oktober 2026
Potassium Hydroxide → 4-(2-carboxy-ethyl)-3-methyl-5-(5-methoxy-2-oxo-1,2-dihydroindol-3-ylidenemethyl)-1H-pyrrole-2-carboxylic acid
https://huagongshe.com/reaction/24548
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Potassium Hydroxide | HCID 14797 | — |
| Edukt | 5-Methoxyoxindole | HCID 1514286 | — |
| Edukt | 5-Formyl-4-(2-ethoxycarbonylethyl)-3-methyl-1H-pyrrole-2-carboxylic acid ethyl ester | HCID 11022333 | — |
| Katalysator | Piperidine | HCID 8082 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | 4-(2-carboxy-ethyl)-3-methyl-5-(5-methoxy-2-oxo-1,2-dihydroindol-3-ylidenemethyl)-1H-pyrrole-2-carboxylic acid | HCID 53913922 | 65% |
Reaktionsschritte
A mixture of 5-formyl-4-(2-ethoxycarbonylethyl)-3-methyl-1H-pyrrole-2-carboxylic acid ethyl ester (562 mg), 5-methoxy-2-oxindole (326 mg), and piperidine (2 drops) in ethanol (2 mL) were stirred at 90° C. for 2 hours. Potassium hydroxide (537 mg) was added, the temperature was increased to 95° C. and held there for 1 hour. The reaction mixture was cooled and concentrated. The residue was dissolved into water and acidified with 2 N hydrochloric acid to pH 2. The precipitate was filtered, washed with water, and dried in a vacuum oven overnight to give 240 mg (65%) of 4-(2-carboxy-ethyl)-3-methyl-5-(5-methoxy-2-oxo-1,2-dihydroindol-3-ylidenemethyl)-1H-pyrrole-2-carboxylic acid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06855730B2 |
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| Quelldatensatz | uspto-grants-2005_02 |
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| ORD ID | ord-330063a5367643f9aae473e6afd267d2 |
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| Quellennotiz | uspto-grants-2005_02 |
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