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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 68177Erstellt: 24. Oktober 2026

N,N-bis(3-aminopropyl)methylamine → N1-Methyl-N3-(3-methyl-4-nitrophenyl)-N1-{3-[(3-methyl-4-nitrophenyl)amino]propyl}-1,3-propanediamine

https://huagongshe.com/de/reaction/68177

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN,N-bis(3-aminopropyl)methylamineHCID 7777—
EduktSodium CarbonateHCID 10340—
Edukt5-Fluoro-2-nitrotolueneHCID 94956—
LösungsmittelTolueneHCID 1140—
ProduktN1-Methyl-N3-(3-methyl-4-nitrophenyl)-N1-{3-[(3-methyl-4-nitrophenyl)amino]propyl}-1,3-propanediamineHCID 86731947—

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08821592B1
Quelldatensatzuspto-grants-2014_09
ORD IDord-727ba28406384fee9d438a866f21cfd8
Quellennotizuspto-grants-2014_09