HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 266602Erstellt: 26. Oktober 2026
Imidazole → N-Cyclooctylperylene-3,4-dicarboximide
https://huagongshe.com/reaction/266602
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Imidazole | HCID 795 | — |
| Edukt | Cyclooctylamine | HCID 2903 | — |
| Edukt | N-(1-Hexylheptyl)perylene-3,4-dicarboximide | HCID 11443487 | — |
| Edukt | Perylene-3,4-dicarboxylic anhydride | HCID 11759069 | — |
| Produkt | N-Cyclooctylperylene-3,4-dicarboximide | HCID 15219583 | — |
Reaktionsschritte
300 mg (0.93 mmol) of perylene-3,4-dicarboxylic anhydride are reacted with 1.5 g (2.15 mmol) of cyclooctylamine and 3 g of imidazole under an argon inert atmosphere at 140° C. for 12 h as in 2c, and the reaction product is worked up and dried in a drying cabinet. To remove unreacted starting material, the product is boiled in 10 per cent potassium carbonate solution and washed with hot water until the filtrate run-off is colourless. The brown-red product is dried in a drying cabinet at 120° C. and then recrystallized by extraction with ethanol. Yield 290 mg (72%) of dark-red crystalline powder without solid fluorescence, m.p. 342°-343° C., Rf (CHCl3 /silica gel)=0.78. UV (CHCl3): λmax (ε)=506 nm (32000), 484 (32100), 264 (35200). Fluorescence (CHCl3) λmax (Irel)=511 nm, 542 (1), 573 (sh, 0.51).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05650513 |
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| Quelldatensatz | uspto-grants-1997_07 |
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| ORD ID | ord-1460794e95284e0c9c8b2ff2d8d1d4c1 |
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| Quellennotiz | uspto-grants-1997_07 |
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