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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 8561생성일: 2026년 10월 24일

Methacrylonitrile → 2-Methyladamantanylmethacrylate methacrylonitrile alpha-butyrolactone methacrylate

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

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참여 물질

역할이름HCID투입량
반응물MethacrylonitrileHCID 31368—
반응물2,2'-Azobis(2-methylbutyronitrile)HCID 93079—
반응물alpha-Butyrolactone MethacrylateHCID 21983218—
반응물2-Methyladamantanyl methacrylateHCID 21983220—
용매TetrahydrofuranHCID 8028—
생성물2-Methyladamantanylmethacrylate methacrylonitrile alpha-butyrolactone methacrylateHCID 86591823—

반응 조건

온도90 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07090968B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-8f56d2638ebd4d958343cc0fd1c539ea
출처 메모uspto-grants-2006_08