反応式
[CH3:1][CH:2]([CH2:6]C)C(=O)C.[C-:8]#[N:9].[K+].C([O:14][CH:15]([CH3:17])[CH3:16])(C)C>C(O)(=O)CC(CC(O)=O)(C(O)=O)O>[OH:14][C@@:15]([CH3:16])([CH2:17][CH:2]([CH3:6])[CH3:1])[C:8]#[N:9]参加物
反応条件
- 温度
- 2.5 °C
実験手順
500 μl of 3-methyl-2-pentanone (4 mmol) were dissolved in 15 ml of diisopropyl ether with stirring, the mixture was cooled to 0-5° C. and an aqueous solution of 520 mg. of potassium cyanide in 20 ml of 0.5 M citric acid was added. After addition of 2 ml of enzyme solution (1000 IU/ml), the reaction vessel was sealed pressure-tight and the mixture was stirred at 0-5° C. for 5 hours. The mixture was then diluted with 30 ml of diisopropyl ether and the reaction mixture was extracted. After separation of the organic phase, the aqueous phase was extracted a second time by shaking with 30 ml of diisopropyl ether. The aqueous phase was discarded, the combined organic phases were dried over anhydrous sodium sulfate and the solvent was removed by distillation under reduced pressure. After column chromatography, 193 mg of (S)-2-hydroxy-2,4-dimethylpentanenitrile (38%) were obtained.
後処理
- additionAfter addition of 2 ml of enzyme solution (1000 IU/ml)
- customthe reaction vessel was sealed pressure-tight
- stirringthe mixture was stirred at 0-5° C. for 5 hours
- extractionthe reaction mixture was extracted
- customAfter separation of the organic phase
- extractionthe aqueous phase was extracted a second time
- stirringby shaking with 30 ml of diisopropyl ether
- dry with materialthe combined organic phases were dried over anhydrous sodium sulfate
- customthe solvent was removed by distillation under reduced pressure
出典と根拠
- ORDレコード
- ord-2cd5d167ca6b4deeb6ed958c1b9684a1
- 出典データセット
- uspto-grants-2002_01
- 特許番号
- US06337196B1
関連ノート
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