참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Methyl Isobutyl Ketone | HCID 7909 | — |
| 반응물 | 4-Methoxystyrene | HCID 12507 | — |
| 반응물 | 2,2'-Azobis(methyl 2-methylpropanate) | HCID 21917503 | — |
| 반응물 | 1-Cyclohexyloxyethyl methacrylate | HCID 22995281 | — |
| 용매 | Heptane | HCID 8900 | — |
| 생성물 | 1-Ethoxy-2-(2-methoxyethoxy)ethane | HCID 13847 | — |
| 생성물 | 1-Cyclohexyloxyethyl methacrylate p-methoxystyrene | HCID 86655543 | — |
반응 단계
Into a 500 ml-volume three-neck flask, 63.7 g (0.30 mol) of 1-cyclohexyloxyethyl methacrylate, 40.3 g (0.30 mol) of p-methoxystyrene 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 ethyl methyl ether, and heptane and methyl isobutyl ketone contained in the solution were removed by distillation under reduced pressure to obtain Polymer A1-6 (1-cyclohexyloxyethyl methacrylate/p-methoxystyrene) as a diethylene glycol ethyl methyl 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-df2f0c3a92004fd3b7a54c24b2283ce0 |
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| 출처 메모 | uspto-grants-2015_05 |
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