HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 617806Erstellt: 25. Oktober 2026
Acetic Acid → 4-Oxo-1,2,3,4-tetrahydro-7H-benzo[c]carbazole-8-carboxylic acid
https://huagongshe.com/reaction/617806
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Acetic Acid | HCID 176 | — |
| Edukt | 2,3-Dichloro-5,6-dicyano-1,4-benzoquinone | HCID 6775 | — |
| Edukt | Benzoic acid, 2-hydrazinyl-, hydrochloride (1:1) | HCID 104169 | — |
| Katalysator | Zincchloride | HCID 3007855 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 4-Oxo-1,2,3,4-tetrahydro-7H-benzo[c]carbazole-8-carboxylic acid | HCID 21849938 | — |
Reaktionsschritte
5.4 g (28.6 mmol) of 2-hydrazinobenzoic acid hydrochloride and 4.7 g (34.3 mmol) of zinc chloride were added to 300 ml of glacial acetic acid. Under stirring at about 85° C., 4.7 g (28.6 mmol) of the compound of Production Example 6 was added thereto over about 5 minutes. Then the obtained mixture was stirred at the same temperature for about 2 hours, brought back to room temperature and the precipitate was recovered by filtration. After concentrating the filtrate, water was added thereto and the precipitate thus formed was recovered by filtration. These precipitates were combined, dried and then dissolved in about 500 ml of dimethylformamide. Under stirring at room temperature, a solution of 6.5 g (28.6 mmol) of 2,3-dichloro-5,6-dicyano-1,4-benzoquinone in tetrahydrofuran (20 ml) was added thereto and the obtained mixture was stirred for about 30 minutes. After concentrating, about 50 ml of ethanol was added and the precipitate thus formed was recovered by filtration to thereby give 3.4 g of the title compound.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05952335 |
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| Quelldatensatz | uspto-grants-1999_09 |
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| ORD ID | ord-8b4671ea111a4c02b29bb02f96d9af51 |
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| Quellennotiz | uspto-grants-1999_09 |
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