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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 35990Erstellt: 24. Oktober 2026

4-Aminophenol → 4-(4-Aminophenoxy)-4'-phenylethynylbenzophenone

https://huagongshe.com/de/reaction/35990

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-AminophenolHCID 403—
EduktTolueneHCID 1140—
EduktPotassium CarbonateHCID 11430—
Edukt4-Fluoro-4'-(phenylethynyl)benzophenoneHCID 4095657—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylacetamideHCID 31374—
Produkt4-(4-Aminophenoxy)-4'-phenylethynylbenzophenoneHCID 2335281385%

Reaktionsbedingungen

Temperatur150 °C

Reaktionsschritte

In a 250 mL flask equipped with nitrogen inlet, overhead stirring assembly, Dean-Stark trap, and reflux condenser were placed 4-aminophenol (5.46 g, 0.05 mol), 4-phenylethynyl-4'-fluorobenzophenone (15.02 g, 0.05 mol), potassium carbonate (7.6 g, 0.055 mol), toluene (20 mL), and DMAc (45 mL). The mixture was heated to 150° C. for 2 h, then cooled to room temperature. The reaction mixture was poured into water and the resulting light yellow powder was collected by filtration. Recrystallization from toluene afforded the desired product in 85% yield: m.p. 151°-153° C. IR (KBr); 3382 and 3314 cm-1 (NH2); 3049, 1599, and 1509 cm-1 (aromatic C--H); 2217 cm-1 (C=C); and 1645 cm-1 (C=O): Mass Spec. m/e (relative intensity): M+, 389.4 (100); FW=389.44 g/mol.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05412066
Quelldatensatzuspto-grants-1995_05
ORD IDord-c9bf34767f6240c1b6e5fc3d71b4a948
Quellennotizuspto-grants-1995_05