HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1618838Generated: October 26, 2026
Glycidyl acrylate → Glycidyl acrylate 2-hydroxyethyl methacrylate p-acetoxystyrene
https://huagongshe.com/reaction/1618838
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Glycidyl acrylate | HCID 7836 | — |
| Reactant | 2-Hydroxyethyl Methacrylate | HCID 13360 | — |
| Reactant | 4-Ethenylphenyl acetate | HCID 75821 | — |
| Reactant | 2,2'-Azobis(methyl 2-methylpropanate) | HCID 21917503 | — |
| Solvent | Methyl Isobutyl Ketone | HCID 7909 | — |
| Solvent | Heptane | HCID 8900 | — |
| Product | Glycidyl acrylate 2-hydroxyethyl methacrylate p-acetoxystyrene | HCID 86655545 | — |
Reaction Steps
A 500 ml three-necked flask was charged with 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. A catalytic amount of 2,2′-azobis(methyl 2-methylpropionate) as a radical polymerization initiator was added to the mixture, and polymerization was performed in a nitrogen stream at 80° C. for six hours. The obtained reaction liquid was cooled, and poured in a large volume of heptane, thereby precipitating a polymer. The polymer crystal was collected by filtration, and dissolved in diethylene glycol dimethyl ether. The heptane and methyl isobutyl ketone contained in the solution were distilled off in vacuum, thereby obtaining a diethylene glycol dimethyl ether solution of polymer A2-2 (glycidyl acrylate/2-hydroxyethyl methacrylate/p-acetoxystyrene).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08771907B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-1bf900b39b3a4f4a8e1f7c993fc931e0 |
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| Source note | uspto-grants-2014_07 |
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