関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Methacrylonitrile | HCID 31368 | — |
| 反応物 | 2,2'-Azobis(2-methylbutyronitrile) | HCID 93079 | — |
| 反応物 | alpha-Butyrolactone Methacrylate | HCID 21983218 | — |
| 反応物 | 2-Methyladamantanyl methacrylate | HCID 21983220 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 2-Methyladamantanylmethacrylate methacrylonitrile alpha-butyrolactone methacrylate | HCID 86591823 | — |
反応手順
2-Methyladamantanyl methacrylate (14.21 g, 0.061 mol), methacrylonitrile (3.05 g, 0.045 mol), and alpha-butyrolactone methacrylate (7.74 g, 0.045 mol) were dissolved in 66 mL of tetrahydrofuran. The resulting colorless solution was deoxygenated by gently bubbling a stream of N2 through the stirring solution for 15 minutes, placed under N2, and heated to 90° C. (oil bath temperature). VAZO67 (0.58 g, 0.0030 mol) dissolved in 7 ml of tetrahydrofuran, was then added to the refluxing mixture over 10 minutes. The polymerization was then refluxed with stirring for 20 hours and cooled to room temperature. The polymer was isolated by precipitation into 800 mL of hexanes, filtered, dried, re-dissolved in 70 mL of tetrahydrofuran, precipitated into 800 mL of hexanes, filtered, washed well with hexanes, and dried in a vacuum oven at 40° C. for 24 hours. Yield 19.8 g (79% of theory). Composition of the title terpolymer was determined by quantitative C-13 NMR and was found to be within experimental error of the monomer feed ratio.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07090968B2 |
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| 出典データセット | uspto-grants-2006_08 |
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| ORD ID | ord-8f56d2638ebd4d958343cc0fd1c539ea |
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| 出典メモ | uspto-grants-2006_08 |
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