Potassium sodium tartarate → 3-(tert-Butyl-dimethyl-silanyloxymethyl)-4-chloro-benzylamine

HRID 1715399笔记

反应方程式

HRID 1715399 反应方程式
[H-].[H-].[H-].[H-].[Li+].[Al+3].[C:7]([SiH2:11][O:12][C:13]([CH3:25])([CH3:24])[C:14]1[CH:15]=[C:16]([CH:20]=[CH:21][C:22]=1[Cl:23])[CH:17]=[N:18]O)([CH3:10])([CH3:9])[CH3:8].C(C(C(C([O-])=O)O)O)([O-])=O.[Na+].[K+]>CCOCC>[C:7]([SiH2:11][O:12][C:13]([CH3:25])([CH3:24])[C:14]1[CH:15]=[C:16]([CH:20]=[CH:21][C:22]=1[Cl:23])[CH2:17][NH2:18])([CH3:10])([CH3:8])[CH3:9]

参与物

5

实验过程

LiAlH4 (4.11 g, 108 mmol) was added in portions to a sol. of 3-(tert-butyl-dimethyl-silanyloxymethyl)-4-chloro-benzaldehyde oxime (13.0 g, 43.4 mmol) in Et2O (433 mL). The mixture was stirred for 1 h at rt. Aq. sat. potassium sodium tartrate (400 mL) was carefully added to the mixture. The mixture was stirred for 3 h, and was extracted with Et2O (3×). The combined org. extracts were dried over MgSO4, filtered, and the solvents were removed under reduced pressure. Drying under high vacuum yielded the crude title compound (12.4 g, quantitative yield) that was used further without purification. LC-MS: tR=0.84 min; ES+: 327.37.

后处理

  1. stirringThe mixture was stirred for 3 h
  2. extractionwas extracted with Et2O (3×)
  3. dry with materialextracts were dried over MgSO4
  4. filtrationfiltered
  5. customthe solvents were removed under reduced pressure
  6. customDrying under high vacuum

来源与证据

ORD记录
ord-488c5bd49f754d488b32d6779546e824
来源数据集
uspto-grants-2010_09
专利号
US07799805B2

反应笔记

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