Réaction #155359

ord-727ba28406384fee9d438a866f21cfd8

Équation de réaction

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

Solvants

Conditions de réaction

Température
100°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

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

Mode opératoire

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).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08821592B1uspto-grants-2014_09