HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 525980Erstellt: 23. Oktober 2026
1-Bromooctane → N1,N1,N5,N5-tetraoctylnaphthalene-1,5-diamine
https://huagongshe.com/de/reaction/525980
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1-Bromooctane | HCID 8140 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 1,5-Diaminonaphthalene | HCID 16720 | — |
| Katalysator | Potassium Iodide | HCID 4875 | — |
| Lösungsmittel | 1-Butanol | HCID 263 | — |
| Produkt | N1,N1,N5,N5-tetraoctylnaphthalene-1,5-diamine | HCID 68441382 | 38,3% |
Reaktionsschritte
Naphthalene-1,5-diamine (3.14 g, 19.8 mmol), 1-bromooctane (25.25 g, 0.130 mol), potassium carbonate (11.79 g, 85.3 mmol), and potassium iodide (0.05 g, 0.30 mmol) was stirred in dry butanol (150 ml) and heated to 110° C. for 36 h. The reaction was quenched with water and extracted with ether three times. The combined organic phase was washed three times with water and evaporated to give black oil which was distilled under reduced pressure at 90° C. to yield a black tar. This was purified with flash chromatography using hexane as mobile phase to obtain colourless oil which crystallised to yield N1,N1,N5,N5-tetraoctylnaphthalene-1,5-diamine (2.3 g, 3.79 mmol) as white crystals. 1H-NMR (CDCl3, δ): 0.85 (t, 12H), 1.0-1.4 (m, 40H), 1.4-1.6 (m, 8H), 3.08 (t, 8H), 7.1 (d, 2H), 7.35 (t, 2H), 8.01 (d, 2H) MS MALDI-TOF (m/z): 606.574
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09343198B2 |
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| Quelldatensatz | uspto-grants-2016_05 |
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| ORD ID | ord-e20de384567c4138967ddc336962212b |
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| Quellennotiz | uspto-grants-2016_05 |
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