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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 266609Erstellt: 24. Oktober 2026

Imidazole → HCID 19033220, Verbindung

https://huagongshe.com/de/reaction/266609

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktImidazoleHCID 795—
Edukt2,5-Ditert-butyl-4-nitroanilineHCID 8167078—
EduktPerylene-3,4-dicarboxylic anhydrideHCID 11759069—
KatalysatorZinc acetate (USP)HCID 2724192—
ProduktHCID 19033220HCID 19033220—

Reaktionsbedingungen

Temperatur170 °C

Reaktionsschritte

0.20 g (0.93 mmol) of perylene-3,4-dicarboxylic anhydride is mixed with 0.47 g (1.9 mmol) of 2,5-di-t-butyl-4-nitroaniline, 0.20 g of zinc acetate dihydrate and 4 g of imidazole, and the mixture is heated under argon at 170° C. for 22 h. The product is removed from the flask by washing with ethanol, treated with 2N hydrochloric acid and then boiled until all the ethanol has evaporated. The solid product is filtered off with suction, washed twice with water and then boiled in 10% potassium carbonate solution. The reaction product is again filtered off with suction while hot and washed several times with hot water until the filtrate run-off is no longer yellow. The residue is dried in a drying cabinet at 120° C. and then chromatographed on silica gel using toluene. The solution thus obtained is filtered through a D5 sintered crucible in order to remove any adhering silica gel. Yield 0.09 g (26%) of a red powder showing a red solid fluorescence, m.p. >360° C., Rf (CHCl3 /silica gel)=0.31, UV (CHCl3): λmax (ε)=514 (24450), 489 (25850), 356 (3100), 265 (33790). Fluorescence (CHCl3): λmax (Ired)=543 (1), 576 (0.45).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05650513
Quelldatensatzuspto-grants-1997_07
ORD IDord-7e5c08cb5ae045478ee1ab69a3852ef0
Quellennotizuspto-grants-1997_07