Reaktion #66195

ord-a6adde18e4e0446c863bbe24ebf188b1

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstige6-Fluoro-3-(2-nitropropenyl)-1H-indole was prepared
  2. 2
    Temperaturto reflux 2 hours
  3. 3
    Waschenwashed with H2O (50 mL×2)
  4. 4
    Sonstigepartitioned
  5. 5
    Trocknendried over Na2SO4
  6. 6
    Filtrationfiltered
  7. 7
    Einengenconcentrated under reduced pressure

Vorschrift

6-Fluoro-3-(2-nitropropenyl)-1H-indole was prepared by combining 6-fluoroindole-3-carboxaldehyde (485 mg, 2.97 mmol), nitroethane (6.0 mL), and ammonium acetate (250 mg, 3.27 mmol). The reaction solution was allowed to reflux 2 hours. The reaction solution was diluted with EtOAc (100 mL), washed with H2O (50 mL×2), partitioned, dried over Na2SO4, filtered, and concentrated under reduced pressure to provide 560 mg (86% yield) of 6-fluoro-3-(2-nitropropenyl)-1H-indole; 1H NMR (CDCl3) δ 11.03 (1H, br s), 8.41 (1H, s), 7.63 (1H, dd), 7.50 (1H, s), 7.06 (1H, dd), 6.92 (1H, t), 2.44 (3H, s); TLC (SiO2 plate, 100% DCM) Rf=0.7.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08524704B2uspto-grants-2013_09