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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanolHCID 887—
EduktStyreneHCID 7501—
EduktN-PhenylmaleimideHCID 13662—
KatalysatorHCID 178501834HCID 178501834—
LösungsmittelTolueneHCID 1140—
Produkt1H-Pyrrole-2,5-dione, 1-phenyl-, polymer with ethenylbenzeneHCID 245901—

Reaktionsbedingungen

Temperatur30 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05262504
Quelldatensatzuspto-grants-1993_11
ORD IDord-4da5cffd3e074836bcebe6e2db5d04e6
Quellennotizuspto-grants-1993_11