참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 4-Ethenylphenyl acetate | HCID 75821 | — |
| 반응물 | 2-((4-Ethenylphenoxy)methyl)oxirane | HCID 102865 | — |
| 반응물 | 1-Ethoxyethyl Methacrylate (stabilized with MEHQ) | HCID 20193345 | — |
| 반응물 | 2,2'-Azobis(methyl 2-methylpropanate) | HCID 21917503 | — |
| 용매 | Methyl Isobutyl Ketone | HCID 7909 | — |
| 용매 | Heptane | HCID 8900 | — |
| 생성물 | p-Vinylphenyl glycidyl ether 1-ethoxyethyl methacrylate p-acetoxystyrene | HCID 86655547 | — |
반응 단계
Into a 500 ml-volume three-neck flask, 52.9 g (0.30 mol) of p-vinylphenyl glycidyl ether, 19.0 g (0.12 mol) of 1-ethoxyethyl methacrylate, 29.2 g (0.18 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 A2-4 (p-vinylphenyl glycidyl ether/1-ethoxyethyl methacrylate/p-acetoxystyrene) as a diethylene glycol dimethyl ether solution.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09034440B2 |
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| 출처 데이터셋 | uspto-grants-2015_05 |
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| ORD ID | ord-384377b14f4e418f88fb24a36393fb6f |
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| 출처 메모 | uspto-grants-2015_05 |
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