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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Aminophenol | HCID 403 | — |
| Reactant | 4-Chloro-8-nitroquinoline | HCID 610440 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(8-Nitroquinolin-4-yloxy)phenylamine | HCID 53330293 | 59% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08049014B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-ed6a338ca328496f9397cccf1be50d07 |
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| Source note | uspto-grants-2011_11 |
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