Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Methanol | HCID 887 | — |
| Edukt | Azobisisobutyronitrile | HCID 6547 | — |
| Edukt | Cyclohexyl acrylate | HCID 18298 | — |
| Edukt | 1-(Tert-butoxy)-4-ethenylbenzene | HCID 577531 | — |
| Lösungsmittel | Isopropanol | HCID 3776 | — |
| Produkt | p-Tert-butoxystyrene cyclohexyl acrylate | HCID 86587325 | — |
Reaktionsschritte
First, 176.3 g (1.0 mol) of p-tert-butoxystyrene and 16.2 g (0.105 mol) of cyclohexyl acrylate were dissolved in 250 ml of isopropanol. In a nitrogen stream, 2,2′-azobisisobutyronitrile was added to the solution, and agitated at 75° C. for six hours. The reaction liquid was cooled, and poured in 5000 ml of an aqueous solution of methanol, thereby precipitating a reaction product. The precipitated solid was collected by filtration, washed with methanol, and dried in vacuum. Thus, 172.5 g of poly(p-tert-butoxystyrene/cyclohexyl acrylate) was obtained as a white powdery crystal.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08642245B2 |
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| Quelldatensatz | uspto-grants-2014_02 |
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| ORD ID | ord-fd69cfff23654517bbdcb8f85511322a |
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| Quellennotiz | uspto-grants-2014_02 |
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