HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1294073Generated: October 29, 2026
4-Aminophenol → 4-(4-Nitrophenoxy)benzenamine
https://huagongshe.com/reaction/1294073
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Aminophenol | HCID 403 | — |
| Reactant | p-Fluoronitrobenzene | HCID 9590 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(4-Nitrophenoxy)benzenamine | HCID 80251 | 99.9% |
Reaction Steps
To a mixture of NaH (60% oily, 880 mg, 22.0 mmol) in DMF (40 mL) was added a solution of 4-aminophenol (2.40 g, 22.0 mmol) in DMF (30 mL) followed by 1-fluoro-4-nitrobenzene (2.12 mL, 20.0 mmol). The mixture was stirred at 90° C. overnight. After cooling, the mixture was extracted with ethyl acetate. The organic layer was washed with water and brine, dried over Na2SO4 then evaporated. Sequence purification on SiO2 column chromatography gave the title compound (4.60 g, quant): MS m/e 229 (M−1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07238813B2 |
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| Source dataset | uspto-grants-2007_07 |
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| ORD ID | ord-6d12f68aa3b149e797ce67dbd8d69613 |
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| Source note | uspto-grants-2007_07 |
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