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N-(2-Methoxyethyl)-2-nitroaniline → 1-N-(2-methoxyethyl)benzene-1,2-diamine

HRID 1096655
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Reaktionsgleichung

Reaktionsgleichung von HRID 1096655
[CH3:1][O:2][CH2:3][CH2:4][NH:5][C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][C:7]=1[N+:12]([O-])=O>CO.C(O)(=O)C.[Zn]>[CH3:1][O:2][CH2:3][CH2:4][NH:5][C:6]1[C:7]([NH2:12])=[CH:8][CH:9]=[CH:10][CH:11]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 1

HCID 10375425N-(2-Methoxyethyl)-2-nitroaniline

Produkt 1

HCID 102614521-N-(2-methoxyethyl)benzene-1,2-diamineAusbeute 72 %

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 23994ZincKatalysatorHCID 176Acetic AcidLösungsmittelHCID 887MethanolLösungsmittel

Versuchsvorschrift

The residue 109A was dissolved in methanol (60 mL) and acetic acid (4 mL). Zinc metal (3.24 g, 49.6 mmol) was added and the mixture was stirred overnight at room temperature. The reaction was decanted off from unreacted zinc metal. The solvent was removed under vacuum and resuspended in ethyl acetate (30 mL). The precipitate was removed by filtration on a Buchner funnel with Celite. Solvent was removed from the filtrate and the residue was purified by column chromatography (2% MeOH/DCM) to give the product N1-(2-methoxyethyl)benzene-1,2-diamine (109B) as a red oil (422 mg, 72% yield over two steps). ESI-MS:m/z 167.4 (M+H)+.

Aufarbeitung

  1. customThe reaction was decanted off from unreacted zinc metal
  2. customThe solvent was removed under vacuum
  3. customThe precipitate was removed by filtration on a Buchner funnel with Celite
  4. customSolvent was removed from the filtrate
  5. customthe residue was purified by column chromatography (2% MeOH/DCM)

Quellen und Nachweise

ORD-Eintrag
ord-46108410ddf843bca44d8d93e7125b22
Quelldatensatz
uspto-grants-2012_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08138168B1

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