反応式
[C:1]1(=[O:7])[O:6][C:4](=[O:5])[CH:3]=[CH:2]1.[CH2:8]=[CH:9][C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1.C(OCC)C>C(C(C)=O)C>[CH2:8]=[CH:9][C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1.[CH:2]1[C:1](=[O:7])[O:6][C:4](=[O:5])[CH:3]=1参加物
反応条件
- 温度
- 60 °C
実験手順
In 200 ml of methyl ethyl ketone were dissolved 19.4 g of maleic anhydride and 20.6 g of styrene, and to the solution was added 0.65 g of azobisisobutylnitrile(AIBN). The resulting mixture was heated at 60° C. for 2 hours under nitrogen atmosphere for performing polymerization. The reaction solution was then dropwise added to 500 ml of ethyl ether under stirring to precipitate a polymer. Thus precipitated polymer was collected by filtration and purified by repeating twice the THF dissolution-ethyl ether precipitation procedure described in Example 1. Thus purified polymer was dried under vacuum at 100° C. for 24 hours to give 31.5 g of a maleic anhydride-styrene copolymer. It was confiremed by elementary analysis that the copolymerization ratio was approximately 1:1. Mn was 55,400.
後処理
- custompolymerization
- customto precipitate a polymer
- filtrationThus precipitated polymer was collected by filtration
- custompurified
- dissolutionthe THF dissolution-ethyl ether precipitation procedure
- customThus purified polymer was dried under vacuum at 100° C. for 24 hours
出典と根拠
- ORDレコード
- ord-cbe89f700d1d4f44be46528cfa737033
- 出典データセット
- uspto-grants-1988_04
- 特許番号
- US04740561
関連ノート
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