関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Methyl Isobutyl Ketone | HCID 7909 | — |
| 反応物 | 4-Methoxystyrene | HCID 12507 | — |
| 反応物 | 2,2'-Azobis(methyl 2-methylpropanate) | HCID 21917503 | — |
| 反応物 | 1-Cyclohexyloxyethyl methacrylate | HCID 22995281 | — |
| 溶媒 | Heptane | HCID 8900 | — |
| 生成物 | 1-Ethoxy-2-(2-methoxyethoxy)ethane | HCID 13847 | — |
| 生成物 | 1-Cyclohexyloxyethyl methacrylate p-methoxystyrene | HCID 86655543 | — |
反応手順
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.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09034440B2 |
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| 出典データセット | uspto-grants-2015_05 |
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| ORD ID | ord-df2f0c3a92004fd3b7a54c24b2283ce0 |
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| 出典メモ | uspto-grants-2015_05 |
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