反応式
[C:1]([O:6][CH3:7])(=[O:5])[C:2](C)=[CH2:3].[C:8](OC[CH:14]([CH3:16])[CH3:15])(=O)[CH:9]=C.[CH2:17](OCNC(=O)C=C)[CH2:18][CH2:19][CH3:20].[C:28]([O:33][CH2:34][CH2:35]O)(=[O:32])[C:29]([CH3:31])=C.C(O)(=O)C=C>>[CH3:17][CH2:18][CH2:19][CH2:20][CH:16]([CH2:7][O:6][C:1]([CH:2]=[CH2:3])=[O:5])[CH2:14][CH3:15].[CH3:8][CH2:9][CH2:35][CH2:34][O:33][C:28]([CH:29]=[CH2:31])=[O:32]参加物
6
実験手順
Except that 30 parts of methyl methacrylate, 198 parts of isobutyl acrylate, 30 parts of N-n-butoxymethylacrylamide, 15 parts of hydroxyethyl methacrylate and 27 parts of acrylic acid were used as the acrylic monomers, synthesis was carried out under conditions similar to those in Synthesis Example 1 to obtain a colorless, transparent resin solution having a solid content of 61%.
後処理
- customin Synthesis Example 1
- customto obtain a colorless, transparent resin solution
出典と根拠
- ORDレコード
- ord-9ef93b145fa74145b94465a46fb80610
- 出典データセット
- uspto-grants-1990_11
- 特許番号
- US04970126
関連ノート
読み込み中…