Potassium Sodium Tartrate → HCID 57205641,化合物
反应方程式
[H-].C([Al+]CC(C)C)C(C)C.[Si:11]([O:18][C@H:19]([C:24]1[CH:29]=[C:28]([Cl:30])[CH:27]=[C:26]([Cl:31])[CH:25]=1)[C:20](OC)=[O:21])([C:14]([CH3:17])([CH3:16])[CH3:15])([CH3:13])[CH3:12].[C@H](O)(C([O-])=O)[C@@H](O)C([O-])=O.[Na+].[K+]>C1(C)C=CC=CC=1.C(OCC)(=O)C>[Si:11]([O:18][C@H:19]([C:24]1[CH:29]=[C:28]([Cl:30])[CH:27]=[C:26]([Cl:31])[CH:25]=1)[CH:20]=[O:21])([C:14]([CH3:17])([CH3:16])[CH3:15])([CH3:13])[CH3:12]参与物
实验过程
Diisobutylaluminum hydride (56.5 mL, 1.5 M in toluene) was added dropwise over 1 h to a cooled (−78° C.) solution of methyl (R)-2-[tert-butyl(dimethyl)silyl]oxy-2-(3,5-dichlorophenyl)ethanoate (14.81 g) in toluene (150 mL) under nitrogen. The resulting colorless solution was stirred at this temperature for 1 h, before a saturated aqueous solution of Rochelle's salt (70 mL) was added dropwise. The resulting mixture was allowed to warm to room temperature, and was then diluted with ethyl acetate. The biphasic system was filtered through celite, rinsing with water and ethyl acetate . The filtrate was separated into its two layers, and the aqueous layer was extracted with ethyl acetate. The extract and the organic layer of the filtrate were combined, washed with saturated aqueous sodium chloride solution, dried (magnesium sulfate), and concentrated to afford (2R)-2-[tert-butyl(dimethyl)silyl]oxy-2-(3,5-dichlorophenyl)ethanal as a colorless oil (13.36 g). Based on its 1H-NMR spectrum, the title compound made up ca. 50% of the oil.
后处理
- additionwas added dropwise
- filtrationThe biphasic system was filtered through celite
- washrinsing with water and ethyl acetate
- customThe filtrate was separated into its two layers
- extractionthe aqueous layer was extracted with ethyl acetate
- extractionThe extract
- washwashed with saturated aqueous sodium chloride solution
- dry with materialdried (magnesium sulfate)
- concentrationconcentrated
来源与证据
- ORD记录
- ord-11b6bde01e9544018c4107f8c276dcd8
- 来源数据集
- uspto-grants-2001_06
- 专利号
- US06251925B1
反应笔记
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