Sodium Hydroxide → 4-(3-chloro-4-fluorophenyl)-1H-indole
反応式
CC1(C)C(C)(C)OB([C:9]2[CH:17]=[CH:16][CH:15]=[C:14]3[C:10]=2[CH:11]=[CH:12][NH:13]3)O1.Br[C:20]1[CH:25]=[CH:24][C:23]([F:26])=[C:22]([Cl:27])[CH:21]=1.[OH-].[Na+]>C1COCC1.[Pd].C(OCC)(=O)C>[Cl:27][C:22]1[CH:21]=[C:20]([C:9]2[CH:17]=[CH:16][CH:15]=[C:14]3[C:10]=2[CH:11]=[CH:12][NH:13]3)[CH:25]=[CH:24][C:23]=1[F:26]参加物
反応条件
- 温度
- 75 °C
実験手順
To a mixture of 4-(4,4,5,5-tetramethyl-[1,3,2) dioxaborolan-2-yl) 1H-indole (3, 3.00 g, 12.34 mmol), and 4-bromo-2-chloro-fluorobenzene (2.58 g, 12.34 mmol) in THF (42 mL)) were added Palladium catalyst Pd(PPh3)4 (0.428 g, 0.37 mmol) and the freshly prepared sodium hydroxide solution (1.50 g, 37.02 mmol in 17 mL water). The system was degassed and then charged with nitrogen. The degas procedure was repeated for three times. The mixture was stirred under nitrogen at 75° C. oil bath for 15 hours. TLC showed the completion of the coupling reaction. The mixture was cooled to room temperature, diluted with ethyl acetate, and separated from water layer. The ethyl acetate solution was washed by brine, dried over Na2SO4, and concentrated. The crude product was purified by a silica gel column eluting with hexanes—EtOAc (9:1) to provide 2.11 g (70%) of the product 43-chloro-4-fluoro-phenyl)-1H-indole as a white solid.
後処理
- customThe system was degassed
- additioncharged with nitrogen
- customthe completion of the coupling reaction
- temperatureThe mixture was cooled to room temperature
- customseparated from water layer
- washThe ethyl acetate solution was washed by brine
- dry with materialdried over Na2SO4
- concentrationconcentrated
- customThe crude product was purified by a silica gel column
- washeluting with hexanes—EtOAc (9:1)
出典と根拠
- ORDレコード
- ord-060f5f2f801f48b6a49a407c80f2fbb8
- 出典データセット
- uspto-grants-2005_03
- 特許番号
- US06861418B2
反応ノート
読み込み中…