反応式
[S:1]([O-:11])([O:4][CH2:5][CH2:6][O:7][CH2:8][CH:9]=[CH2:10])(=[O:3])=[O:2].[C:12](I)([C:15]([C:18]([C:21]([C:24]([C:27]([C:30]([C:33]([F:36])([F:35])[F:34])([F:32])[F:31])([F:29])[F:28])([F:26])[F:25])([F:23])[F:22])([F:20])[F:19])([F:17])[F:16])([F:14])[F:13]>>[S:1]([OH:11])([O:4][CH2:5][CH2:6][O:7][CH2:8][CH:9]=[CH:10][C:12]([F:14])([F:13])[C:15]([F:16])([F:17])[C:18]([F:19])([F:20])[C:21]([F:22])([F:23])[C:24]([F:25])([F:26])[C:27]([F:29])([F:28])[C:30]([F:32])([F:31])[C:33]([F:36])([F:35])[F:34])(=[O:2])=[O:3]参加物
3
実験手順
Crystalline allyloxyethyl sulfate (Na salt) from the preparation shown in example 2 was perfluoroalkylated using the procedure of example 7 and C8F17I to produce 2-(4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,11-heptadecafluoroundec-2-enyloxy)ethyl hydrogen sulfate.
出典と根拠
- ORDレコード
- ord-9ce66c0ac6a9497f90fd9e34b54bd9d0
- 出典データセット
- uspto-grants-2013_09
- 特許番号
- US08524104B1
関連ノート
読み込み中…