Hydrogen Bromide → 4-(2-Bromo-2,2-difluoro-ethyl)-pyrrolidin-2-one
反応式
[F:1][C:2]([F:10])=[CH:3][CH:4]1[CH2:8][NH:7][C:6](=[O:9])[CH2:5]1.[BrH:11]>O>[Br:11][C:2]([F:10])([F:1])[CH2:3][CH:4]1[CH2:8][NH:7][C:6](=[O:9])[CH2:5]1参加物
4
実験手順
In a 50 ml three necked flask fitted with a magnetic stirrer, under inert atmosphere, 0.1 g of 4-(2,2-difluoro-vinyl)-pyrrolidin-2-one a5 (0.6 mmol) is heated in HBr (62% w/w in H2O, 10 ml) for 0.75 h at reflux. The reaction mixture is cooled down to room temperature, diluted with water and extracted with CH2Cl2 (3 times), dried over MgSO4, filtered and concentrated in vacuo to afford 0.076 g of 4-(2-bromo-2,2-difluoro-ethyl)-pyrrolidin-2-one a6 (49%).
後処理
- temperatureat reflux
- extractionextracted with CH2Cl2 (3 times)
- dry with materialdried over MgSO4
- filtrationfiltered
- concentrationconcentrated in vacuo
出典と根拠
- ORDレコード
- ord-14a74e31c8124ad5afc98a56028857ab
- 出典データセット
- uspto-grants-2010_07
- 特許番号
- US07763644B2
反応ノート
読み込み中…