関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 2-Hydroxyethyl Methacrylate | HCID 13360 | — |
| 反応物 | 4-Ethenylphenyl acetate | HCID 75821 | — |
| 反応物 | Tetrahydropyranyl methacrylate | HCID 11041138 | — |
| 反応物 | 2,2'-Azobis(methyl 2-methylpropanate) | HCID 21917503 | — |
| 溶媒 | Methyl Isobutyl Ketone | HCID 7909 | — |
| 溶媒 | Heptane | HCID 8900 | — |
| 生成物 | Propylene glycol methyl ether acetate | HCID 7946 | — |
| 生成物 | 1-Ethoxy-2-(2-methoxyethoxy)ethane | HCID 13847 | — |
| 生成物 | 2-Tetrahydropyranyl methacrylate p-acetoxystyrene 2-hydroxyethyl methacrylate | HCID 86657623 | — |
反応手順
Into a 500 ml-volume three-neck flask, 71.5 g (0.42 mol) of 2-tetrahydropyranyl methacrylate, 19.5 g (0.12 mol) of p-acetoxystyrene, 7.8 g (0.06 mol) of 2-hydroxyethyl 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 a mixed solvent of propylene glycol monomethyl ether acetate and 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 A1-7 (2-tetrahydropyranyl methacrylate/p-acetoxystyrene/2-hydroxyethyl methacrylate) as a solution in a mixed solvent of propylene glycol monomethyl ether acetate and diethylene glycol ethyl methyl ether.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US09034440B2 |
|---|
| 出典データセット | uspto-grants-2015_05 |
|---|
| ORD ID | ord-0f00b9825d854a42998bbc8a14935fbe |
|---|
| 出典メモ | uspto-grants-2015_05 |
|---|