反応式
[F:1][C:2]([F:17])([S:13]([OH:16])(=[O:15])=[O:14])[C:3]([F:12])([F:11])[C:4]([F:10])([F:9])[C:5]([F:8])([F:7])[F:6].[OH-].[CH2:19]([N+:26]([CH3:29])([CH3:28])[CH3:27])[C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1>>[CH2:19]([N+:26]([CH3:29])([CH3:28])[CH3:27])[C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1.[F:17][C:2]([F:1])([S:13]([O-:16])(=[O:15])=[O:14])[C:3]([F:11])([F:12])[C:4]([F:10])([F:9])[C:5]([F:8])([F:7])[F:6]参加物
3
実験手順
Perfluorobutanesulfonic acid benzyltrimethylammonium salt is prepared by neutralising perfluorobutanesulfonic acid and benzyltrimethylammonium hydroxide in aqueous solution. Benzyltrimethylammonium hydroxide is obtainable from Aldrich.
出典と根拠
- ORDレコード
- ord-72007794f9f04d989d5f2583f29f5ba0
- 出典データセット
- uspto-grants-2007_01
- 特許番号
- US07169333B2
関連ノート
読み込み中…