HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 257550Erstellt: 24. Oktober 2026
Methanol → 1H-Pyrrole-2,5-dione, 1-phenyl-, polymer with ethenylbenzene
https://huagongshe.com/de/reaction/257550
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Methanol | HCID 887 | — |
| Edukt | Styrene | HCID 7501 | — |
| Edukt | N-Phenylmaleimide | HCID 13662 | — |
| Katalysator | HCID 178501834 | HCID 178501834 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | 1H-Pyrrole-2,5-dione, 1-phenyl-, polymer with ethenylbenzene | HCID 245901 | — |
Reaktionsschritte
In a 0.5-liter reactor equipped with a stirrer were placed 100 ml of styrene and 6.0 mmol as aluminum atom of methylaluminoxane obtained in the above Example 1 (1), and the resultant was stirred at the polymerization temperature of 30° C. for 30 minutes. Subsequently, 0.03 mmol as titanium atom of pentamethylcyclopentadienyltitanium trimethoxide was added. At the same time, 100 g of N-phenylmaleimide was dissolved in 300 ml of toluene, and after sufficiently replaced with nitrogen, this solution was added and polymerization was carried out at 40° C. for 5 hours with stirring. After the reaction was over, methanol was poured to stop the reaction. Further, a mixture of methanolhydrochloric acid was added to decompose the catalyst components. Then, washing with methanol was repeated three times. The yield of thus obtained styrene-N-phenylmaleimide copolymer was 51.5 g. Intrinsic viscosity measured in 1,2,4-trichlorobenzene at 135° C. was 0.66 dl/g.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05262504 |
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| Quelldatensatz | uspto-grants-1993_11 |
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| ORD ID | ord-4da5cffd3e074836bcebe6e2db5d04e6 |
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| Quellennotiz | uspto-grants-1993_11 |
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