반응 #586100

ord-62388dac03b24cc1990f6196e9532ce6

반응 방정식

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
수율 88.0%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    여과The catalyst was filtered off
  2. 2
    기타after evaporation of the solvent
  3. 3
    기타the product was chromatographed on silacagel (eluent: 10% ethylacetate in hexane)

실험 절차

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.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07767623B2uspto-grants-2010_08