Ethyl isobutyrate → Ethyl 4-chloro-2,2-dimethylbutanoate
反応式
C(NC(C)C)(C)C.C([Li])CCC.[C:13]([O:18][CH2:19][CH3:20])(=[O:17])[CH:14]([CH3:16])[CH3:15].Br[CH2:22][CH2:23][Cl:24].[Cl-].[NH4+]>O1CCCC1.CCCCCC>[Cl:24][CH2:23][CH2:22][C:14]([CH3:16])([CH3:15])[C:13]([O:18][CH2:19][CH3:20])=[O:17]参加物
反応条件
- 温度
- -78 °C
実験手順
To a solution of 22.2 ml of diisopropylamine in 150 ml of tetrahydrofuran being stirred, 93.6 ml of a 1.6 M solution of n-butyl lithium in hexane was added at -5° to 0° C., followed by stirring for 30 minutes. After the reaction mixture was cooled to -78° C. and 19.0 ml of ethyl isobutyrate was added dropwise to the mixture and stirred for 45 minutes. A solution of 11.9 ml of 1-bromo-2-chloroethane in 10 ml of tetrahydrofuran was added dropwise to the reaction mixture. After the reaction mixture was stirred at -78° C. for 1 hour and then at roomtemperature (15° to 20° C.) for 2 hours, an excess amount of an aqueous solution of ammonium chloride was added, followed by extractionwith ethyl acetate. After the extract was washed with water and dried over MgSO4, the solvent was distilled off; the residue was then distilled under reduced pressure, to yield 24.7 g of the title compound in the form of a colorless oily substance.
後処理
- stirringstirred for 45 minutes
- stirringAfter the reaction mixture was stirred at -78° C. for 1 hour
- waitat roomtemperature (15° to 20° C.) for 2 hours
- extractionfollowed by extractionwith ethyl acetate
- washAfter the extract was washed with water
- dry with materialdried over MgSO4
- distillationthe solvent was distilled off
- distillationthe residue was then distilled under reduced pressure
出典と根拠
- ORDレコード
- ord-6788a144a8f145d0899ed1b1e9de313d
- 出典データセット
- uspto-grants-1996_02
- 特許番号
- US05491145
反応ノート
読み込み中…