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HRID 1291939Erstellt: 23. Oktober 2026
Water → 2,5-Bis[4-(3,4-dimethyl-5-isoxazolyl)sulfamoylanilino]terephthalic acid
https://huagongshe.com/de/reaction/1291939
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Water | HCID 962 | — |
| Edukt | Sulfuric Acid | HCID 1118 | — |
| Edukt | Sulfisoxazole | HCID 5344 | — |
| Edukt | Potassium Hydroxide | HCID 14797 | — |
| Edukt | Sodium 3-nitrobenzenesulfonate | HCID 31389 | — |
| Edukt | Dimethylsuccinyl succinate | HCID 131720661 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | 2,5-Bis[4-(3,4-dimethyl-5-isoxazolyl)sulfamoylanilino]terephthalic acid | HCID 18913708 | 70,4% |
Reaktionsschritte
To 150 g of methanol was added with stirring 20 g (87.6 mmol) of dimethylsuccinyl succinate, 53.9 g (201.6 mmol) of 4-amino-N-(3,4-dimethyl-5-isoxazolyl)benzenesulfonamide (Aldrich Chemical Co.), and 0.7 g of concentrated sulfuric acid. The reaction mixture was heated slowly to 95° to 97° C. and maintained at that temperature for five hours. After the reaction mixture was cooled to 50° C., 26 g of sodium 3-nitrobenzenesulfonate, 2 g of water, and 75 g of 45% aqueous potassium hydroxide were slowly added with stirring. The resultant mixture was then slowly heated to 90° C and maintained at that temperature for four hours. The reaction mixture was cooled to room temperature and added to 500 ml of water. Concentrated sulfuric acid was slowly added to produce a solid that was collected by filtration and washed with water. The wet presscake was dried in an oven to give 43 g (70.4% of theory) of 2,5-bis[4-(3,4-dimethyl-5-isoxazolyl)sulfamoylanilino]terephthalic acid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05755873 |
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| Quelldatensatz | uspto-grants-1998_05 |
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| ORD ID | ord-5bf4fed710744353ab0975c0e0ea28b7 |
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| Quellennotiz | uspto-grants-1998_05 |
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