反応式
[F:1][C:2]([F:17])([S:13]([O-: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].[K+].[Br-].[O:20]=[C:21]([C:28]([CH3:31])([CH3:30])[CH3:29])[CH2:22][S+:23]1[CH2:27][CH2:26][CH2:25][CH2:24]1.C(OCC)(=O)C>O.CO>[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].[O:20]=[C:21]([C:28]([CH3:31])([CH3:30])[CH3:29])[CH2:22][S+:23]1[CH2:27][CH2:26][CH2:25][CH2:24]1参加物
6
実験手順
In a mixed solvent of 500 ml of water and 100 ml of methanol was dissolved 10 g of potassium perfluorobutanesulfonate, and to the solution was added a solution containing 7.75 g of 2-oxo-3,3-dimethylbutyltetrahydrothiophenium bromide dissolved in 50 ml of methanol. The aqueous solution was extracted twice with each 100 ml of chloroform, and the organic phase was washed with water and concentrated to obtain an oily product. To the oily product was added ethyl acetate, and the solution was again concentrated to obtain a solid product. The solid product was collected by filtration and subjected to reslurry with diisopropyl ether to obtain 9 g of 2-oxo-3,3-dimethylbutyltetrahydrothiophenium perfluorobutanesulfonate.
後処理
- additionto the solution was added a solution
- extractionThe aqueous solution was extracted twice with each 100 ml of chloroform
- washthe organic phase was washed with water
- concentrationconcentrated
- customto obtain an oily product
- concentrationthe solution was again concentrated
- customto obtain a solid product
- filtrationThe solid product was collected by filtration
出典と根拠
- ORDレコード
- ord-b67ff457c9c04f028399ffa57e7c4806
- 出典データセット
- uspto-grants-2004_10
- 特許番号
- US06808862B2
関連ノート
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