참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2-Hydroxyethyl Methacrylate | HCID 13360 | — |
| 반응물 | 2-((4-Ethenylphenoxy)methyl)oxirane | HCID 102865 | — |
| 반응물 | Tetrahydropyranyl methacrylate | HCID 11041138 | — |
| 반응물 | 2,2'-Azobis(methyl 2-methylpropanate) | HCID 21917503 | — |
| 용매 | Methyl Isobutyl Ketone | HCID 7909 | — |
| 용매 | Heptane | HCID 8900 | — |
| 생성물 | 1-Ethoxy-2-(2-methoxyethoxy)ethane | HCID 13847 | — |
| 생성물 | 2-Tetrahydropyranyl methacrylate p-vinylphenyl glycidyl ether 2-hydroxyethyl methacrylate | HCID 86643211 | — |
반응 단계
A 500 ml three-necked flask was charged with 57.0 g (0.36 mol) of 2-tetrahydropyranyl methacrylate, 31.7 g (0.18 mol) of p-vinylphenyl glycidyl ether, 7.8 g (0.06 mol) of 2-hydroxyethyl methacrylate 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 ethyl methyl ether. The heptane and methyl isobutyl ketone contained in the solution were distilled off in vacuum, thereby obtaining a diethylene glycol ethyl methyl ether solution of polymer A-6 (2-tetrahydropyranyl methacrylate/p-vinylphenyl glycidyl ether/2-hydroxyethyl methacrylate).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08771907B2 |
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| 출처 데이터셋 | uspto-grants-2014_07 |
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| ORD ID | ord-469d1e6d52d8497ab63599fba065b556 |
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| 출처 메모 | uspto-grants-2014_07 |
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