Ammonium Chloride → 2-(4,4-Dimethyl-3,4-dihydroquinolin-1(2H)-yl)aniline

HRID 2192212

Reaktionsgleichung

Reaktionsgleichung von HRID 2192212
[CH3:1][C:2]1([CH3:21])[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[N:5]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=2[N+:18]([O-])=O)[CH2:4][CH2:3]1.[NH4+].[Cl-]>CO.[Zn]>[CH3:1][C:2]1([CH3:21])[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[N:5]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=2[NH2:18])[CH2:4][CH2:3]1

Komponenten

5

Edukt 2

HCID 25517Ammonium ChlorideHCID 574233104,4-Dimethyl-1-(2-nitrophenyl)-1,2,3,4-tetrahydroquinoline

Produkt 1

HCID 593377072-(4,4-Dimethyl-3,4-dihydroquinolin-1(2H)-yl)anilineAusbeute 73 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 23994ZincKatalysatorHCID 887MethanolLösungsmittel

Versuchsvorschrift

The crude 1c (0.66 g) was stirred in MeOH (20 mL) at rt. Solid NH4Cl (0.62 g) was added, followed by addition of Zn dust (3.0 g) portionwise. The resulting mixture was stirred at rt for 2 h. It was filtered through Celite®, rinsed with CH2Cl2, and concentrated to dryness. The residue was purified by flash chromatography (hexanes/EtOAc) to give pure amine 1d (0.43 g, 73% for two steps). LC-MS ESI 253 (M+H).

Aufarbeitung

  1. filtrationIt was filtered through Celite®
  2. washrinsed with CH2Cl2
  3. concentrationconcentrated to dryness
  4. customThe residue was purified by flash chromatography (hexanes/EtOAc)

Quellen und Nachweise

ORD-Eintrag
ord-766cb1a34b974b689e5e6e5f8a63d2f9
Quelldatensatz
uspto-grants-2012_12
Patentnummer
US08329718B2

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