Azobisisobutyronitrile → HCID 86609791、化合物
反応式
[C:1]([O:5][C:6](=[O:9])[CH:7]=[CH2:8])([CH3:4])([CH3:3])[CH3:2].[F:10][C:11]([F:18])([F:17])[C:12](=[CH2:16])[C:13]([OH:15])=[O:14].[C:19]([O:24][CH2:25][C:26]([F:34])([F:33])[CH:27]([F:32])[C:28]([F:31])([F:30])[F:29])(=[O:23])[C:20]([CH3:22])=[CH2:21].CC(N=NC(C#N)(C)C)(C#N)C>CC(C)=O>[C:1]([O:5][C:6](=[O:9])[CH:7]=[CH2:8])([CH3:4])([CH3:3])[CH3:2].[F:10][C:11]([F:18])([F:17])[C:12](=[CH2:16])[C:13]([OH:15])=[O:14].[C:19]([O:24][CH2:25][C:26]([F:33])([F:34])[CH:27]([F:32])[C:28]([F:30])([F:31])[F:29])(=[O:23])[C:20]([CH3:22])=[CH2:21]参加物
6
実験手順
5 g of t-butylacrylate, 2.5 g of 2-(trifluoromethyl)acrylic acid, 2.5 g of 2,2,3,4,4,4-hexafluorobutyl methacrylate and 0.2 g of AIBN were dissolved in 50 g of acetone. The monomers were polymerized at 67° C. for 6 hours. After completion of the polymerization, the polymerization product was precipitated in water, filtered, and dried in a vacuum to give poly(t-butylacrylate-2-(trifluoromethyl)acrylic acid-2,2,3,4,4,4-hexafluorobutyl methacrylate) (yield: 75%) of Formula 3, below:
後処理
- customThe monomers were polymerized at 67° C. for 6 hours
- customAfter completion of the polymerization
- customthe polymerization product was precipitated in water
- filtrationfiltered
- customdried in a vacuum
出典と根拠
- ORDレコード
- ord-dcc1c8070e17481484919492943cc6a6
- 出典データセット
- uspto-grants-2008_12
- 特許番号
- US07462439B2
反応ノート
読み込み中…