HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1425628Generated: November 1, 2026
Benzyl methacrylate → 1-Ethoxyethyl methacrylate (1-ethyl-3-oxacyclobutyl)methyl methacrylate benzyl methacrylate
https://huagongshe.com/reaction/1425628
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzyl methacrylate | HCID 17236 | — |
| Reactant | (3-Ethyloxetan-3-yl)methyl 2-methylprop-2-enoate | HCID 11159706 | — |
| Reactant | 1-Ethoxyethyl Methacrylate (stabilized with MEHQ) | HCID 20193345 | — |
| Reactant | 2,2'-Azobis(methyl 2-methylpropanate) | HCID 21917503 | — |
| Solvent | Methyl Isobutyl Ketone | HCID 7909 | — |
| Solvent | Heptane | HCID 8900 | — |
| Product | 1-Ethoxyethyl methacrylate (1-ethyl-3-oxacyclobutyl)methyl methacrylate benzyl methacrylate | HCID 86643213 | — |
Reaction Steps
Into a 500 ml-volume three-neck flask, 47.5 g (0.3 mol) of 1-ethoxyethyl methacrylate, 33.2 g (0.18 mol) of (1-ethyl-3-oxacyclobutyl)methyl methacrylate, 21.2 g (0.12 mol) of benzyl methacrylate 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 A-8 (1-ethoxyethyl methacrylate/(1-ethyl-3-oxacyclobutyl)methyl methacrylate/benzyl methacrylate) as a diethylene glycol dimethyl ether solution.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08932800B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-ba4619f136d54d39a7f9ce801a19c2df |
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| Source note | uspto-grants-2015_01 |
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