反応式
[OH:1][C:2]1[CH:10]=[C:9]2[C:5]([CH2:6][CH2:7][C:8]2=[O:11])=[CH:4][C:3]=1[O:12][CH3:13].C(=O)([O-])[O-].[K+].[K+].Br[CH2:21][CH2:22][CH2:23][C:24]([O:26][CH2:27][CH3:28])=[O:25]>CC(C)=O>[CH3:13][O:12][C:3]1[CH:4]=[C:5]2[C:9]([C:8](=[O:11])[CH2:7][CH2:6]2)=[CH:10][C:2]=1[O:1][CH2:21][CH2:22][CH2:23][C:24]([O:26][CH2:27][CH3:28])=[O:25]参加物
反応条件
- 温度
- 60 °C
実験手順
To a stirred solution of 6-hydroxy-5-methoxy-2,3-dihydro-1H-inden-1-one 18a (0.01 mol, 1.78 g) in acetone (50 ml) was added potassium carbonate (0.02 mol, 2.80 g). The resulting mixture was refluxed for 2 hours. After cooling to room temperature ethyl 4-bromobutyrate was added. The reaction mixture was stirred at 60° C. for 12 h. The progress of the reaction was monitored by TLC. The reaction mixture was filtered and the precipitate was washed with acetone (15 ml×2). The combined filtrate was concentrated on rotavapor and the residue was diluted with ethyl acetate. The ethyl acetate solution was successively washed with water, saturated sodium bicarbonate (Na2HCO3), water and dried over magnesium sulfate (Mg2SO4). After evaporation of the solvent the crude product was purified by passing through a short silica gel column using 0-50% gradient of ethyl acetate and hexane as eluent to give the pure indanone as colorless thick liquid in 30% yield (0.87 g). 1H NMR (400 MHz, CDCl3): δ 1.21 (3H, broad t); 2.16 (2H, m); 2.44 (2H, m); 2.59 (2H, m); 2.96 (2H, m); 3.93 (3H, s); 4.04 (2H, broad t); 4.10 (2H, broad q); 6.84 (1H, m); 7.43 (1H, s); 7.12 (1H, s). MS (ESI): m/z=293.20 (M+H+).
後処理
- temperatureThe resulting mixture was refluxed for 2 hours
- additionwas added
- filtrationThe reaction mixture was filtered
- washthe precipitate was washed with acetone (15 ml×2)
- concentrationThe combined filtrate was concentrated on rotavapor
- additionthe residue was diluted with ethyl acetate
- washThe ethyl acetate solution was successively washed with water, saturated sodium bicarbonate (Na2HCO3), water
- dry with materialdried over magnesium sulfate (Mg2SO4)
- customAfter evaporation of the solvent the crude product
- customwas purified
出典と根拠
- ORDレコード
- ord-fc2478e9050d45f283c88a34ce974eea
- 出典データセット
- uspto-grants-2013_11
- 特許番号
- US08580822B2
関連ノート
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