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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1450012Generated: October 26, 2026

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

https://huagongshe.com/reaction/1450012

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-AminophenolHCID 403—
ReactantTolueneHCID 1140—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Fluoro-4'-(phenylethynyl)benzophenoneHCID 4095657—
SolventWaterHCID 962—
SolventDimethylacetamideHCID 31374—
Product4-(4-Aminophenoxy)-4'-phenylethynylbenzophenoneHCID 2335281385%

Reaction Conditions

Temperature150 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05599993
Source datasetuspto-grants-1997_02
ORD IDord-c9d3ff532c3a426aac71f9b92bc0b5ed
Source noteuspto-grants-1997_02