HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 525981Erstellt: 26. Oktober 2026
1,5-Dihydroxynaphthalene → 1,5-Bis(octyloxy)naphthalene
https://huagongshe.com/reaction/525981
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1,5-Dihydroxynaphthalene | HCID 6749 | — |
| Edukt | 1-Bromooctane | HCID 8140 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 1,5-Bis(octyloxy)naphthalene | HCID 50901175 | 140,2% |
Reaktionsschritte
1,5-dihydroxynaphthalene (2.95 g, 18.4 mmol), 1-bromooctane (8.2 g, 42.5 mmol), and potassium carbonate (50 g, 0.36 mol) was mixed in N,N-dimethylformamide and heated at 90° C. for 5 h. The potassium carbonate was filtered off and the reaction mixture was quenched with water and extracted two times with ether. The combined organic phase was then washed once with 1M HCl, two times with water, and evaporated. The residual brown solid was recrystallised in ethanol to form 1,5-bis(octyloxy)naphthalene (4.96 g, 12.9 mmol) as brown crystals. 1H-NMR (CDCl3, δ): 0.89 (t, 6H), 1.2-1.4 (m, 16H), 1.4-1.6 (m, 4H), 1.91 (m, 4H), 4.12 (t, 4H), 6.81 (d, 2H), 7.34 (t, 2H), 7.83 (d, 2H) MS MALDI-TOF (m/z): 384.266
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-9909275f86894bd9a2aaf61545134d1e |
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| Quellennotiz | uspto-grants-2016_05 |
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