反応式
[F:1][C:2]([F:10])([C:6]([F:9])([F:8])[F:7])[C:3](Cl)=[O:4].N1C=CC=CC=1.[CH:17]([O:19][CH2:20][CH2:21][CH2:22][CH3:23])=[CH2:18].O>ClCCl>[CH2:20]([O:19][CH:17]=[CH:18][C:3](=[O:4])[C:2]([F:10])([F:1])[C:6]([F:9])([F:8])[F:7])[CH2:21][CH2:22][CH3:23]参加物
6
反応条件
- 温度
- -10 °C
実験手順
With stirring at −10° C., 17.0 g (93.2 mmol) of pentafluoropropionyl chloride—dissolved in 20 ml of dichloromethane—were added to a mixture of 8.11 g (102 mmol) pyridine and 9.33 g (93.2 mmol) of butyl vinyl ether in 200 ml of dichloromethane. After the addition, stirring was continued at room temperature for a further 15 h. 200 ml of water were then added to the mixture, and the organic phase was separated off, dried and concentrated. This gave 18.9 g (82% of theory) of a yellowish oil.
後処理
- additionAfter the addition
- stirringstirring
- customthe organic phase was separated off
- customdried
- concentrationconcentrated
出典と根拠
- ORDレコード
- ord-aa141b5811d04a5db4f0e3b86a915386
- 出典データセット
- uspto-grants-2015_08
- 特許番号
- US09102623B2
関連ノート
読み込み中…