Reaktion #4140

ord-be31b5d785ad45829427ebbf59eaec37

Reaktionsgleichung

O=[N+]([O-])c1cc(Br)ccc1N1CCCc2ccccc21
1-(4-Bromo-2-nitrophenyl)-1,2,3,4-tetrahydroquinoline
CCO
ethanol
Nc1cc(Br)ccc1N1CCCc2ccccc21
product
Ausbeute 100.0%
Nc1cc(Br)ccc1N1CCCc2ccccc21
1-(4-Bromo-2-aminophenyl)-1,2,3,4-tetrahydroquinoline
Ausbeute 100.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    FiltrationThe mixture was filtered
  2. 2
    Sonstigethe filtrate was evaporated at 50° C. under vacuum

Vorschrift

1-(4-Bromo-2-nitrophenyl)-1,2,3,4-tetrahydroquinoline (11.6 g, 0.035 mole) was dissolved in benzene (125 ml), and ethanol added (75 ml), followed by 1% platinum-on-charcoal (0.40 g). The mixture was shaken under an initial pressure of 56 psi for 6.5 hours. The mixture was filtered and the filtrate was evaporated at 50° C. under vacuum to provide 10.6 g (100%) of product, as a gum.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04723007uspto-grants-1988_02