반응 #4198

ord-3ebfa7b3c5cb47f9828c4e52f9823e21

반응 방정식

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

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    여과The mixture was filtered
  2. 2
    기타the filtrate was evaporated at 50° C. under vacuum

실험 절차

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.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US04723003uspto-grants-1988_02