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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2302126Erstellt: 25. Oktober 2026

Cyclohexyl acrylate → p-Tert-butoxystyrene cyclohexyl acrylate

https://huagongshe.com/reaction/2302126

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCyclohexyl acrylateHCID 18298—
Edukt1-(Tert-butoxy)-4-ethenylbenzeneHCID 577531—
Edukt2,2'-Azobis(methyl 2-methylpropanate)HCID 21917503—
LösungsmittelMethanolHCID 887—
Lösungsmittel1,4-DioxaneHCID 31275—
Produktp-Tert-butoxystyrene cyclohexyl acrylateHCID 86587325—

Reaktionsschritte

To 50 g (0.284 mole) of p-tert-butoxystyrene and 43.8 g (0.284 mole) of cyclohexyl acrylate was added 3 g of 2,2′-azobis(methyl 2-methylpropionate), followed by conducting a polymerization reaction in 1,4-dioxane under nitrogen gas streams at 80° C. for 6 hours. After cooling, the reaction solution was poured in 5000 ml of aqueous methanol solution to precipitate out. Crystal was recovered by filtration and dried under reduced pressure to give 89.2 g of poly(p-tert-butoxystyrene/cyclohexyl acrylate) as white powdery crystal. A weight-average molecular weight of the polymer was about 21000 by GPC measurement using polystyrene as a standard.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06432608B1
Quelldatensatzuspto-grants-2002_08
ORD IDord-d810103e678f47d596aee3a7c20b8322
Quellennotizuspto-grants-2002_08