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HRID 840496作成日:2026年10月27日

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

反応式

関与物質

役割名称HCID仕込み量
反応物AzobisisobutyronitrileHCID 6547—
反応物Maleic AnhydrideHCID 7923—
反応物3-(Tris(trimethylsiloxy)silyl)propyl methacrylateHCID 123371—
反応物Bicyclo[2.2.1]hept-5-ene-2-carboxylic acid, 1,1-dimethylethyl esterHCID 15607334—
反応物Mono-2-ethyl-2-(hydroxymethyl)butyl bicyclo-[2.2.1]hept-5-ene-2,3-dicarboxylateHCID 86757924—
溶媒TetrahydrofuranHCID 8028—
生成物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 methacrylateHCID 86757923—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06368771B1
出典データセットuspto-grants-2002_04
ORD IDord-f453fa0f25164914b5f276ce420bb989
出典メモuspto-grants-2002_04