反応式
C(NC(C)C)(C)C.C([Li])CCC.[Br:13][C:14]1[CH:15]=[C:16]([F:20])[CH:17]=[CH:18][CH:19]=1.[Cl-].[NH4+].[O:23]1CCC[CH2:24]1>O.CN(C)C=O>[Br:13][C:14]1[CH:19]=[CH:18][CH:17]=[C:16]([F:20])[C:15]=1[CH:24]=[O:23]参加物
実験手順
To a solution of diisopropylamine (2.65 mL) in tetrahydrofuran (30 mL) was added n-butyllithium (2.44 mol/L n-hexane solution, 7.03 mL) at −78° C. under an argon atmosphere, and the mixture was stirred at the same temperature for 5 minutes. To the reaction mixture was added 3-bromofluorobenzene (3 g), and the mixture was stirred at the same temperature for 1 hour. To the reaction mixture was added N,N-dimethylformamide (1.45 mL), and the mixture was stirred at the same temperature for 10 minutes, then a saturated ammonium chloride aqueous solution was added to the reaction mixture, and the mixture was stirred under ice-cooling for 5 minutes. The mixture was poured into water, and the mixture was extracted with diethyl ether. The extract washed with water and brine and dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure to give the title compound (3.43 g).
後処理
- stirringthe mixture was stirred at the same temperature for 1 hour
- stirringthe mixture was stirred at the same temperature for 10 minutes
- stirringthe mixture was stirred under ice-
- temperaturecooling for 5 minutes
- extractionthe mixture was extracted with diethyl ether
- washThe extract washed with water and brine
- dry with materialdried over anhydrous magnesium sulfate
- customthe solvent was removed under reduced pressure
出典と根拠
- ORDレコード
- ord-9b32939980df43e6b1eb49e473bef3e4
- 出典データセット
- uspto-grants-2010_06
- 特許番号
- US07732596B2
関連ノート
読み込み中…