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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 266602Erstellt: 26. Oktober 2026

Imidazole → N-Cyclooctylperylene-3,4-dicarboximide

https://huagongshe.com/reaction/266602

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktImidazoleHCID 795—
EduktCyclooctylamineHCID 2903—
EduktN-(1-Hexylheptyl)perylene-3,4-dicarboximideHCID 11443487—
EduktPerylene-3,4-dicarboxylic anhydrideHCID 11759069—
ProduktN-Cyclooctylperylene-3,4-dicarboximideHCID 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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05650513
Quelldatensatzuspto-grants-1997_07
ORD IDord-1460794e95284e0c9c8b2ff2d8d1d4c1
Quellennotizuspto-grants-1997_07