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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2083859Generated: October 25, 2026

Cyclohexyl acrylate → p-Tert-butoxystyrene cyclohexyl acrylate

https://huagongshe.com/reaction/2083859

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexyl acrylateHCID 18298—
Reactant1-(Tert-butoxy)-4-ethenylbenzeneHCID 577531—
Reactant2,2'-Azobis(methyl 2-methylpropanate)HCID 21917503—
SolventMethanolHCID 887—
Solvent1,4-DioxaneHCID 31275—
Productp-Tert-butoxystyrene cyclohexyl acrylateHCID 86587325—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06716573B2
Source datasetuspto-grants-2004_04
ORD IDord-a65b8d5bed8646e7892b049cdc34dca5
Source noteuspto-grants-2004_04