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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | N,N-bis(3-aminopropyl)methylamine | HCID 7777 | — |
| Edukt | Sodium Carbonate | HCID 10340 | — |
| Edukt | 5-Fluoro-2-nitrotoluene | HCID 94956 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | N1-Methyl-N3-(3-methyl-4-nitrophenyl)-N1-{3-[(3-methyl-4-nitrophenyl)amino]propyl}-1,3-propanediamine | HCID 86731947 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08821592B1 |
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| Quelldatensatz | uspto-grants-2014_09 |
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| ORD ID | ord-727ba28406384fee9d438a866f21cfd8 |
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| Quellennotiz | uspto-grants-2014_09 |
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