HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 976180Erstellt: 24. Oktober 2026
Bis(3-aminopropyl)amine → Bis(3-{[(4-methylphenyl)sulfonyl]amino}propyl)[(4-methylphenyl)sulfonyl]amine
https://huagongshe.com/de/reaction/976180
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Bis(3-aminopropyl)amine | HCID 5942 | — |
| Edukt | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Lösungsmittel | Pyridine | HCID 1049 | — |
| Produkt | Bis(3-{[(4-methylphenyl)sulfonyl]amino}propyl)[(4-methylphenyl)sulfonyl]amine | HCID 373797 | 59% |
Reaktionsschritte
To a stirred solution of p-toluenesulfonyl chloride (240 g, 1.26 mole) in pyridine (600 ml) at 0° C. was added a solution of 1,5,9-triazanonane (50.0 g, 0.381 mole) in pyridine (100 ml) under a dry nitrogen atmosphere, maintaining the temperature ≤60° C. The addition required 15 minutes. The solvent was removed in vacuo and the resulting yellow oil was dissolved in ethyl acetate (1 l) and H2O (500 ml). The ethyl acetate layer was separated, washed with 0.1N HCl, H2O and saturated NaCl solution and dried (MgSO4). The solution was decolorized with silica gel and the solvent was removed in vacuo to give 133 g (59% yield) of the crude product as a glassy solid: 1H NMR (CDCl3) δ1.71 (quint, J=6.6 Hz, 4 H), 2.42 (s, 6 H), 2.43 (s, 3 H), 2.96 (quart, J=6.4 Hz, 4 H), 3.11 (t, J=6.8 Hz, 4 H), 5.12 (t, J=6.6 Hz, 2 H), 7.30 (m, 6 H), 7.63 (m, 2 H), 7.73 (m, 4 H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05610293 |
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| Quelldatensatz | uspto-grants-1997_03 |
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| ORD ID | ord-8a1496379aea4c7c9c64f669c0b49a23 |
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| Quellennotiz | uspto-grants-1997_03 |
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