반응 #2383778
ord-1047302d657c4c47b2d228796d2cf922
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후처리
- 1기타equipped with a thermometer, a condenser pipe, and a nitrogen inlet pipe
- 2온도the mixture was heated
- 3온도under reflux at 70 C
- 4workup.ADDITIONwhile introducing nitrogen for 8 hr
- 5기타polymerization
- 6기타After the completion of the polymerization
- 7기타to precipitate the resultant polymer, which
- 8기타was then dried
실험 절차
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 70 C. 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: