Reaktion #155359

ord-727ba28406384fee9d438a866f21cfd8

Reaktionsgleichung

Cc1cc(F)ccc1[N+](=O)[O-]
5-fluoro-2-nitrotoluene
O=C([O-])[O-].[Na+].[Na+]
sodium carbonate
CN(CCCN)CCCN
3,3′-Diamino-N-methyldipropylamine
Cc1cc(NCCCN(C)CCCNc2ccc([N+](=O)[O-])c(C)c2)ccc1[N+](=O)[O-]
N1-Methyl-N3-(3-methyl-4-nitrophenyl)-N1-{3-[(3-methyl-4-nitrophenyl)-amino]propyl}-1,3-propanediamine

Lösungsmittel

Reaktionsbedingungen

Temperatur
100°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstige(exothermic reaction)
  2. 2
    Sonstigeto precipitate
  3. 3
    Filtrationwhich were filtered off
  4. 4
    EinengenThe organic phase was then concentrated down under vacuum in a rotovap
  5. 5
    Sonstigeto afford the product as a residue in the form of a yellow orange oil

Vorschrift

To 5-fluoro-2-nitrotoluene (50.0 g, 0.32 mol) was added sodium carbonate (17.1 g, 0.16 mol) at 60° C. 3,3′-Diamino-N-methyldipropylamine (23.7 g, 0.16 mol) was then carefully added dropwise (exothermic reaction). The resulting mixture was heated at 100° C. for 12 hours. 100 ml toluene were added to the cooled reaction mixture causing the inorganic salts to precipitate, which were filtered off. The organic phase was then concentrated down under vacuum in a rotovap to afford the product as a residue in the form of a yellow orange oil. Yield: 52.5 g (78.4%); 1H-NMR (400 MHz, DMSO-d6): δ [ppm]=1.71 (m, 4H); 2.18 (s, 3H); 2.40 (m, 4H); 2.55 (s, 6H); 3.17 (m, 4H); 6.45 (s, 2H); 6.48 (d, 2H); 7.08 (br., 2×NH); 7.92 (d, 2H).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08821592B1uspto-grants-2014_09