反応式
[F:1][C:2]1[CH:11]=[C:10]2[C:5]([C:6](=O)[CH2:7][C:8]([CH3:13])([CH3:12])[O:9]2)=[CH:4][CH:3]=1.C[Si](C#N)(C)C.[C:21]([O:24]CC)(=[O:23])C>Cl.[I-].[Zn+2].[I-]>[F:1][C:2]1[CH:11]=[C:10]2[C:5]([CH:6]([C:21]([OH:24])=[O:23])[CH2:7][C:8]([CH3:13])([CH3:12])[O:9]2)=[CH:4][CH:3]=1参加物
反応条件
- 温度
- 50 °C
実験手順
To 7-fluoro-2,2-dimethyl-2,3-dihydrochromen-4-one (1.000 g, 5.149 mmol) was added trimethylsilyl cyanide (3.215 mL, 25.75 mmol) followed by a spatula tip of zinc iodide. The reaction was heated at 50° C. for 1 hour. The reaction was cooled, diluted with ethyl acetate (40 mL) and washed with saturated sodium bicarbonate (2×25 mL), brine (25 mL), dried over magnesium sulfate and concentrated. The product was dissolved in 5 mL of acetic acid and 5 mL of HCl, and SnCl2 dihydrate (4.648 g, 20.60 mmol) was added. The reaction heated at reflux (130° C. oil bath temperature) overnight. The reaction was cooled, diluted with ethyl acetate (50 mL), washed with water (50 mL) and brine (50 mL), dried over magnesium sulfate and concentrated. The residue was purified by silica gel chromatography over silica gel eluting with a gradient of 0.5% MeOH/CH2Cl2 containing 0.5% acetic acid to 10% MeOH/CH2Cl2 containing 0.5% acetic acid to provide the title compound (0.280 g, 24.25% yield).
後処理
- temperatureThe reaction was cooled
- washwashed with saturated sodium bicarbonate (2×25 mL), brine (25 mL)
- dry with materialdried over magnesium sulfate
- concentrationconcentrated
- dissolutionThe product was dissolved in 5 mL of acetic acid
- temperatureThe reaction heated
- temperatureat reflux (130° C. oil bath temperature) overnight
- temperatureThe reaction was cooled
- washwashed with water (50 mL) and brine (50 mL)
- dry with materialdried over magnesium sulfate
- concentrationconcentrated
- customThe residue was purified by silica gel chromatography over silica gel eluting with a gradient of 0.5% MeOH/CH2Cl2 containing 0.5% acetic acid to 10% MeOH/CH2Cl2 containing 0.5% acetic acid
出典と根拠
- ORDレコード
- ord-150d4e245b7741a38f0706ab981a186d
- 出典データセット
- uspto-grants-2014_05
- 特許番号
- US08716498B2
関連ノート
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