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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 554480Generated: October 30, 2026

4-Aminophenol → 4-(8-Nitroquinolin-4-yloxy)phenylamine

https://huagongshe.com/reaction/554480

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-AminophenolHCID 403—
Reactant4-Chloro-8-nitroquinolineHCID 610440—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
Product4-(8-Nitroquinolin-4-yloxy)phenylamineHCID 5333029359%

Reaction Conditions

Temperature110 °C

Reaction Steps

4-Chloro-8-nitroquinoline (176 mg, 0.85 mmol) and 4-aminophenol (93 mg, 0.85 mmol) were dissolved in dimethylformamide, and to which 1.0 M potassium tert-butoxide (0.95 mL) in tetrahydrofuran was slowly added dropwise at room temperature, which was then heated and stirred at 110° C. for seven hours. When the reaction was completed, the resultant was extracted with ethyl acetate and aqueous sodium chloride, and the combined organic layers were dried with anhydrous sodium sulfate, and then filtered. The solvent was removed by vacuum distillation, and the residue was purified by a column chromatography (ethyl acetate/n-hexane=½) to obtain 140.6 mg of the desired compound as a reddish brown solid (yield 59.0%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08049014B2
Source datasetuspto-grants-2011_11
ORD IDord-ed6a338ca328496f9397cccf1be50d07
Source noteuspto-grants-2011_11