反応式
Br[C:2]1[CH:3]=[C:4]([CH2:8][CH2:9][OH:10])[CH:5]=[CH:6][CH:7]=1.C[NH:12][CH2:13][CH2:14]NC.[C:17](=[O:20])([O-])[O-:18].[K+].[K+].[Cl-].[NH4+]>O1CCOCC1.[Cu]I>[OH:10][CH2:9][CH2:8][C:4]1[CH:3]=[C:2]([N:12]2[CH2:13][CH2:14][O:18][C:17]2=[O:20])[CH:7]=[CH:6][CH:5]=1参加物
反応物 4
生成物 1
試薬・触媒・溶媒 2
反応条件
- 温度
- 100 °C
実験手順
A solution 2-(3-bromophenyl)ethanol (1.00 g, 5.00 mmol), 2-oxazolidin-2-one (874 mg, 10.04 mmol), copper(I)iodide (96 mg, 0.50 mmol), N,N′-dimethyl-1,2-ethanediamine (60 μL, 49 mg, 0.56 mmol) and potassium carbonate (1.04 g, 7.50 mmol) were suspended in dioxane (6 mL). The mixture was stirred under nitrogen for 2.5 h at 100° C. After addition of copper(I)iodide (96 mg, 0.50 mmol) and N,N′-dimethyl-1,2-ethanediamine (60 μl, 49 mg, 0.56 mmol) stirring was continued for another 2 h at 100° C. After cooling down to room temperature, the mixture was poured into saturated aqueous ammonium chloride solution and extracted with dichloromethane. The organic layer was dried over magnesium sulfate and concentrated under reduced pressure. The crude compound was purified by flash chromatography on silica gel, eluting with ethyl acetate-cyclohexane (1:1 to 1:0) affording the title compound in 64% yield (664 mg).
後処理
- stirringstirring
- waitwas continued for another 2 h at 100° C
- temperatureAfter cooling down to room temperature
- extractionextracted with dichloromethane
- dry with materialThe organic layer was dried over magnesium sulfate
- concentrationconcentrated under reduced pressure
- customThe crude compound was purified by flash chromatography on silica gel
- washeluting with ethyl acetate-cyclohexane (1:1 to 1:0)
出典と根拠
- ORDレコード
- ord-3e987077da3849439d683577127ec598
- 出典データセット
- uspto-grants-2010_06
- 特許番号
- US07732600B2
関連ノート
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