関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Maleic Anhydride | HCID 7923 | — |
| 反応物 | Tetrahydrofuran | HCID 8028 | — |
| 触媒 | Azobisisobutyronitrile | HCID 6547 | — |
| 溶媒 | Hexane | HCID 8058 | — |
| 生成物 | Furan-2,5-dione;5-methylidenebicyclo[2.2.1]hept-2-ene | HCID 287853 | 183.7% |
反応手順
This synthesis example is directed to the synthesis of polymer (1b) (illustrated below as chemical formulas 14 or 15), a γ-hydroxy carboxylic acid structure. 21.2 g of 5-ethylenebicyclo[2.2.1]hept-2-ene, 19.6 g of maleic anhydride, 2.56 g of 2,2'-azobisisobutyronitrile, and 240 g of tetrahydrofuran were placed in a 500-ml, three-necked flask equipped with a thermometer, a condenser pipe, and a nitrogen inlet pipe, and the mixture was heated under reflux at 70C while introducing nitrogen for 8 hr to conduct polymerization. After the completion of the polymerization, the reaction mixture was poured into 1000 ml of n-hexane to precipitate the resultant polymer, which was then dried to give 37.5 g of a 5-methylenebicyclo[2.2.1]hept-2-ene/maleic anhydride copolymer (1a) (yield 92%). The polymer was analyzed by various methods and was found to mainly have a structure represented by the following formula:
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06156486 |
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| 出典データセット | uspto-grants-2000_12 |
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| ORD ID | ord-dd1ec775283349cc88a233305065aec9 |
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| 出典メモ | uspto-grants-2000_12 |
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