反应 #586100

ord-62388dac03b24cc1990f6196e9532ce6

反应方程式

CC(=C[Si](C)(C)C)c1ccccc1[N+](=O)[O-]
product
CC(=C[Si](C)(C)C)c1ccccc1[N+](=O)[O-]
2-(2-Nitrophenyl)-3-(trimethylsilyl)-2-propene
[H][H]
hydrogen
CC(C[Si](C)(C)C)c1ccccc1N
2-(2-aminophenyl)-3-(trimethylsilyl)-propane
收率 88.0%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    过滤The catalyst was filtered off
  2. 2
    其他after evaporation of the solvent
  3. 3
    其他the product was chromatographed on silacagel (eluent: 10% ethylacetate in hexane)

实验过程

The reaction product of step A [7.2 g] was hydrogenated in tetrahydrofurane over palladium on charcoal at atmospheric pressure and room temperature until the uptake of hydrogen ceased. The catalyst was filtered off and, after evaporation of the solvent, the product was chromatographed on silacagel (eluent: 10% ethylacetate in hexane) to yield 2-(2-aminophenyl)-3-(trimethylsilyl)-propane [4.7 g; 88% purity according to NMR]. This product was used in the next step without further purification.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07767623B2uspto-grants-2010_08