化工社化工社 化学情報印刷レポート · 研究参考用
HRID 2191185作成日:2026年10月25日
2-Hydroxyethyl Methacrylate → 1-Cyclohexyloxyethyl methacrylate 3,4-epoxycyclohexylmethyl methacrylate 2-hydroxyethyl methacrylate
https://huagongshe.com/reaction/2191185
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 2-Hydroxyethyl Methacrylate | HCID 13360 | — |
| 反応物 | (7-Oxabicyclo(4.1.0)heptan-3-yl)methyl 2-methylprop-2-enoate | HCID 14645478 | — |
| 反応物 | 2,2'-Azobis(methyl 2-methylpropanate) | HCID 21917503 | — |
| 反応物 | 1-Cyclohexyloxyethyl methacrylate | HCID 22995281 | — |
| 溶媒 | Methyl Isobutyl Ketone | HCID 7909 | — |
| 溶媒 | Heptane | HCID 8900 | — |
| 生成物 | 1-Cyclohexyloxyethyl methacrylate 3,4-epoxycyclohexylmethyl methacrylate 2-hydroxyethyl methacrylate | HCID 86643210 | — |
反応手順
Into a 500 ml-volume three-neck flask, 76.4 g (0.36 mol) of 1-cyclohexyloxyethyl methacrylate, 35.3 g (0.18 mol) of 3,4-epoxycyclohexylmethyl methacrylate (Cyclomer M100, produced by Daicel Chemical Industries, Ltd.), 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 diethylene glycol dimethyl ether, and heptane and methyl isobutyl ketone contained in the solution were removed by distillation under reduced pressure to obtain Polymer A-5 (1-cyclohexyloxyethyl methacrylate/3,4-epoxycyclohexylmethyl methacrylate/2-hydroxyethyl methacrylate) as a diethylene glycol dimethyl ether solution.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08329380B2 |
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| 出典データセット | uspto-grants-2012_12 |
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| ORD ID | ord-effc43291b5a4d58bf5cfcb7ee348b26 |
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| 出典メモ | uspto-grants-2012_12 |
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