反応式
[NH2:1][CH:2]([CH2:6][CH3:7])[C:3]([OH:5])=[O:4].C(N(CC)CC)C.C[Si](Cl)(C)C.[C:20](Cl)(=[O:24])[CH2:21][CH2:22][CH3:23].[OH-].[Na+]>ClCCl.O>[C:20]([NH:1][CH:2]([CH2:6][CH3:7])[C:3]([OH:5])=[O:4])(=[O:24])[CH2:21][CH2:22][CH3:23]参加物
反応条件
- 温度
- 0 °C
実験手順
25.78 g of 2-aminobutyric acid (250 mmol) and 55.66 g (550 mmol) of triethylamine are dissolved in 250 ml of dichloromethane, and the solution is cooled to 0° C. 59.75 g (550 mmol) of trimethylsilyl chloride are added dropwise, and the solution is stirred at room temperature for 1 hour and at 40° C. for one hour. After cooling to −10° C., 26.64 g (250 mmol) of butyryl chloride are added dropwise, and the resulting mixture is stirred at −10° C. for 2 hours and at room temperature for one hour. With ice-cooling, 125 ml of water are added dropwise, and the reaction mixture is stirred at room temperature for 15 minutes. Aqueous sodium hydroxide solution is added to the organic phase, and the organic solvent is removed under reduced pressure. The residue is acidified and the precipitated solid is triturated once with water and twice with petroleum ether and dried under reduced pressure at 45° C. 29.1 g (67%) of a colorless solid.
後処理
- temperatureAfter cooling to −10° C.
- stirringthe resulting mixture is stirred at −10° C. for 2 hours and at room temperature for one hour
- temperatureWith ice-cooling
- stirringthe reaction mixture is stirred at room temperature for 15 minutes
- customthe organic solvent is removed under reduced pressure
- customthe precipitated solid is triturated once with water and twice with petroleum ether
- customdried under reduced pressure at 45° C
出典と根拠
- ORDレコード
- ord-46b5a06419784ab4aa0ab701d258a09a
- 出典データセット
- uspto-grants-2006_08
- 特許番号
- US07098207B2
関連ノート
読み込み中…