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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 840496생성일: 2026년 10월 26일

Azobisisobutyronitrile → Maleic anhydride mono-2-ethyl-2-(hydroxymethyl)butyl bicyclo[2.2.1]hept-5-ene-2.3-dicarboxylate tert-butyl bicyclo-[2.2.1]hept-5-ene-2-carboxylate 3-[tris(trimethylsiloxy)silyl]propyl methacrylate

https://huagongshe.com/reaction/840496

반응식

참여 물질

역할이름HCID투입량
반응물AzobisisobutyronitrileHCID 6547—
반응물Maleic AnhydrideHCID 7923—
반응물3-(Tris(trimethylsiloxy)silyl)propyl methacrylateHCID 123371—
반응물Bicyclo[2.2.1]hept-5-ene-2-carboxylic acid, 1,1-dimethylethyl esterHCID 15607334—
반응물Mono-2-ethyl-2-(hydroxymethyl)butyl bicyclo-[2.2.1]hept-5-ene-2,3-dicarboxylateHCID 86757924—
용매TetrahydrofuranHCID 8028—
생성물Maleic anhydride mono-2-ethyl-2-(hydroxymethyl)butyl bicyclo[2.2.1]hept-5-ene-2.3-dicarboxylate tert-butyl bicyclo-[2.2.1]hept-5-ene-2-carboxylate 3-[tris(trimethylsiloxy)silyl]propyl methacrylateHCID 86757923—

반응 단계

1.0 mole of maleic anhydride, 0.2 mole of mono-2-ethyl-2-(hydroxymethyl)butyl bicyclo-[2.2.1]hept-5-ene-2,3-dicarboxylate, 0.7 mole of tert-butyl bicyclo-[2.2.1]hept-5-ene-2-carboxylate and 0.1 mole of 3-[tris(trimethylsiloxy)silyl]propyl methacrylate are dissolved in tetrahydrofuran, 0.5 to 10 g of AIBN is added thereto as the polymerization initiator, and the resultant mixture is reacted at approximately 60 to 70° C. for 4 to 24 hours under a nitrogen or argon atmosphere.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06368771B1
출처 데이터셋uspto-grants-2002_04
ORD IDord-f453fa0f25164914b5f276ce420bb989
출처 메모uspto-grants-2002_04