Ethanol → 5-Bromo-2-[3,4-dihydro-1(2H)-quinolinyl]aniline

HRID 34391

Reaktionsgleichung

Reaktionsgleichung von HRID 34391
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]2[C:17]3[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=3)[CH2:11][CH2:10][CH2:9]2)=[C:4]([N+:18]([O-])=O)[CH:3]=1.C(O)C>C1C=CC=CC=1.[Pt]>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]2[C:17]3[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=3)[CH2:11][CH2:10][CH2:9]2)=[C:4]([NH2:18])[CH:3]=1

Komponenten

5

Edukt 2

HCID 702EthanolHCID 138129271-(4-Bromo-2-nitrophenyl)-1,2,3,4-tetrahydroquinoline

Produkt 1

HCID 138129315-Bromo-2-[3,4-dihydro-1(2H)-quinolinyl]anilineAusbeute 100 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 23939PlatinumKatalysatorHCID 241BenzeneLösungsmittel

Versuchsvorschrift

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.

Aufarbeitung

  1. filtrationThe mixture was filtered
  2. customthe filtrate was evaporated at 50° C. under vacuum

Quellen und Nachweise

ORD-Eintrag
ord-910f83bd82b942f7813c50e79f694656
Quelldatensatz
uspto-grants-1988_08
Patentnummer
US04761412

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