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HRID 8561作成日:2026年10月23日

Methacrylonitrile → 2-Methyladamantanylmethacrylate methacrylonitrile alpha-butyrolactone methacrylate

https://huagongshe.com/ja/reaction/8561

反応式

関与物質

役割名称HCID仕込み量
反応物MethacrylonitrileHCID 31368—
反応物2,2'-Azobis(2-methylbutyronitrile)HCID 93079—
反応物alpha-Butyrolactone MethacrylateHCID 21983218—
反応物2-Methyladamantanyl methacrylateHCID 21983220—
溶媒TetrahydrofuranHCID 8028—
生成物2-Methyladamantanylmethacrylate methacrylonitrile alpha-butyrolactone methacrylateHCID 86591823—

反応条件

温度90 °C

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US07090968B2
出典データセットuspto-grants-2006_08
ORD IDord-8f56d2638ebd4d958343cc0fd1c539ea
出典メモuspto-grants-2006_08