Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Methanol | HCID 887 | — |
| Edukt | 1-Ethenyl-4-methylbenzene | HCID 12161 | — |
| Edukt | 1-(Tert-butoxy)-4-ethenylbenzene | HCID 577531 | — |
| Edukt | 2,2'-Azobis(methyl 2-methylpropanate) | HCID 21917503 | — |
| Lösungsmittel | 1,4-Dioxane | HCID 31275 | — |
| Produkt | p-Tert-butoxystyrene p-methylstyrene | HCID 67612459 | — |
Reaktionsschritte
To a solution of 100 g (0.567 mol) of p-tert-butoxystyrene and 3.54 g (0.03 mol) of p-methylstyrene in 300 ml of 1,4-dioxane was added a catalytic amount of 2,2'-azobis(methyl 2-methylpropionate) to carry out reaction in a nitrogen stream at 80° for 6 hours. The reaction solution was cooled and poured into 5,000 ml of a methanol solution to cause crystallization. Precipitated crystals were filtered out, washed with methanol and dried in vacuo to give 92.3 g of poly-(p-tert-butoxystyrene/p-methylstyrene)as white powder. The polymer was found to have p-tert-butoxystyrene unit and p-methylstyrene unit in a molar ratio of ca. 95:5 based on 1H NMR. The weight-average molecular weight (Mw) was determined to be about 20,000 by GPC with polystyrene calibration.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05976759 |
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| Quelldatensatz | uspto-grants-1999_11 |
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| ORD ID | ord-bf44012fb98d40d38f3334174e1d2dba |
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| Quellennotiz | uspto-grants-1999_11 |
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