反応式
[C:1]([C:5]1[CH:10]=[CH:9][C:8]([OH:11])=[CH:7][C:6]=1[Cl:12])([CH3:4])([CH3:3])[CH3:2].C(=O)([O-])[O-].[K+].[K+].Br[CH2:20][C:21]([O:23][C:24]([CH3:27])([CH3:26])[CH3:25])=[O:22]>CC(C)=O>[C:1]([C:5]1[CH:10]=[CH:9][C:8]([O:11][CH2:20][C:21]([O:23][C:24]([CH3:27])([CH3:26])[CH3:25])=[O:22])=[CH:7][C:6]=1[Cl:12])([CH3:4])([CH3:2])[CH3:3]参加物
5
反応条件
- 温度
- 65 °C
実験手順
To an acetone (5 ml) solution of 4-tert-butyl-3-chlorophenol (440 mg, 2.4 mmol) were added potassium carbonate (994 mg, 7.2 mmol) and tert-butyl bromoacetate (0.7 ml, 4.8 mmol). The stirred mixture was refluxed at 65° C. for 14 hours. The precipitate was filtered off and washed with acetone. The filtrate was concentrated under reduced pressure to give a residue, which was applied to a silica gel chromatography column and eluted with ethyl acetate/hexane= 1/9 to furnish 0.83 g (100% yield) of the title as a colorless oil.
後処理
- filtrationThe precipitate was filtered off
- washwashed with acetone
- concentrationThe filtrate was concentrated under reduced pressure
- customto give a residue, which
- washeluted with ethyl acetate/hexane= 1/9
- customto furnish 0.83 g (100% yield) of the title as a colorless oil
出典と根拠
- ORDレコード
- ord-2ea319d3e09e435f8d9d2ad2f7f08dbb
- 出典データセット
- uspto-grants-2007_05
- 特許番号
- US07214824B2
関連ノート
読み込み中…