Maleic Anhydride → 2-Hydroxyethyl oxabicyclo[2,2,1]hept-5-ene-2-carboxylate t-butyl 5-norbornene-2-carboxylate maleic anhydride
반응식
[CH:1]12[CH2:7][CH:4]([CH:5]=[CH:6]1)[O:3][CH:2]2[C:8]([O:10][CH2:11][CH2:12][OH:13])=[O:9].[CH:14]12[CH2:20][CH:17]([CH:18]=[CH:19]1)[CH2:16][CH:15]2[C:21]([O:23][C:24]([CH3:27])([CH3:26])[CH3:25])=[O:22].[C:28]1(=[O:34])[O:33][C:31](=[O:32])[CH:30]=[CH:29]1>O1CCCC1>[CH:1]12[CH2:7][CH:4]([CH:5]=[CH:6]1)[O:3][CH:2]2[C:8]([O:10][CH2:11][CH2:12][OH:13])=[O:9].[CH:14]12[CH2:20][CH:17]([CH:18]=[CH:19]1)[CH2:16][CH:15]2[C:21]([O:23][C:24]([CH3:27])([CH3:26])[CH3:25])=[O:22].[C:31]1(=[O:32])[O:33][C:28](=[O:34])[CH:29]=[CH:30]1참가 물질
5
반응물 3
생성물 1
시약·촉매·용매 1
실험 절차
2-hydroxyethyl oxabicyclo[2,2,1]hept-5-ene-2-carboxylate (0.15 mol), t-butyl 5-norbornene-2-carboxylate (0.85 mol), and maleic anhydride (1 mol) were dissolved in a tetrahydrofuran solvent. 2,2-azobisisobutyonitrile (5.84 g) was added, and the solution was mixed. The solution was polymerized at a temperature of 67° C. in a nitrogen atmosphere for 10 hours. After the polymerization reaction was completed, the polymer was precipitated in an ethyl ether solvent, then dried in a vacuum to obtain the pure title polymer (63.94 g). (yield: 22%, purity: 99.9%).
후처리
- additionthe solution was mixed
- customThe solution was polymerized at a temperature of 67° C. in a nitrogen atmosphere for 10 hours
- customAfter the polymerization reaction
- customthe polymer was precipitated in an ethyl ether solvent
- customdried in a vacuum
출처 및 근거
- ORD 기록
- ord-4fd7717d03774bdf8be00243ec5b75de
- 출처 데이터셋
- uspto-grants-2002_07
- 특허 번호
- US06416926B1
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