反应方程式
[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]参与物
反应条件
- 温度
- 0 °C
实验过程
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.
后处理
- 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
来源与证据
- ORD记录
- ord-46b5a06419784ab4aa0ab701d258a09a
- 来源数据集
- uspto-grants-2006_08
- 专利号
- US07098207B2
关联笔记
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