Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 4-Aminophenol | HCID 403 | — |
| Edukt | Dimethylformamide | HCID 6228 | — |
| Edukt | Maleic Anhydride | HCID 7923 | — |
| Edukt | Phosphorus oxide (P4O10) | HCID 14812 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 1-(4-hydroxyphenyl)-1H-pyrrole-2,5-dione | HCID 81734 | 48,4% |
Reaktionsschritte
In a reactor, 30.0 g (0.275 moles) of p-aminophenol, 29.7 g (0.303 moles) of maleic anhydride, 39.0 g (0.275 moles) of phosphorus pentoxide and 100 g of dimethylformamide were charged and stirred at 15° C. for 2 hours. The reaction mixture was then gradually heated to 60° C., at which temperature the reaction was further continued for 2.5 hours. After cooling to room temperature, the resulting reaction mixture was admixed with water to precipitate N-(p-hydroxyphenyl) maleimide in the form of crystals. The crystals were separated by filtration, washed with water and then dried to obtain 25.1 g (0.133 moles) of N-(p-hydroxyphenyl) maleimide (yield 48.2%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04231934 |
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| Quelldatensatz | uspto-grants-1980_11 |
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| ORD ID | ord-0c376d98037b459695cb4da196558734 |
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| Quellennotiz | uspto-grants-1980_11 |
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