HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 574026Erstellt: 24. Oktober 2026
Glycidyl acrylate → Glycidyl acrylate 2-hydroxyethyl methacrylate p-acetoxystyrene
https://huagongshe.com/de/reaction/574026
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Glycidyl acrylate | HCID 7836 | — |
| Edukt | 2-Hydroxyethyl Methacrylate | HCID 13360 | — |
| Edukt | 4-Ethenylphenyl acetate | HCID 75821 | — |
| Edukt | 2,2'-Azobis(methyl 2-methylpropanate) | HCID 21917503 | — |
| Lösungsmittel | Methyl Isobutyl Ketone | HCID 7909 | — |
| Lösungsmittel | Heptane | HCID 8900 | — |
| Produkt | Glycidyl acrylate 2-hydroxyethyl methacrylate p-acetoxystyrene | HCID 86655545 | — |
Reaktionsschritte
Into a 500 ml-volume three-neck flask, 46.1 g (0.36 mol) of glycidyl acrylate, 15.6 g (0.12 mol) of 2-hydroxyethyl methacrylate, 19.5 g (0.12 mol) of p-acetoxystyrene and 300 ml of methyl isobutyl ketone were charged. A catalytic amount of 2,2′-azobis(methyl 2-methylpropionate) was added thereto as a radical polymerization initiator, and polymerization was allowed to proceed at 80° C. for 6 hours in a nitrogen stream. The reaction solution was cooled and then poured in a large amount of heptane to precipitate a polymer. The crystal was collected by filtration and dissolved in diethylene glycol dimethyl ether, and heptane and methyl isobutyl ketone contained in the solution were removed by distillation under reduced pressure to obtain Polymer A2-2 (glycidyl acrylate/2-hydroxyethyl methacrylate/p-acetoxystyrene) as a diethylene glycol dimethyl ether solution.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09034440B2 |
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| Quelldatensatz | uspto-grants-2015_05 |
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| ORD ID | ord-07cc3b10779746bcb3093aa6e64a7431 |
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| Quellennotiz | uspto-grants-2015_05 |
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