HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 29880Generated: October 26, 2026
4-Fluorophenol → 3-(4-Fluorophenoxy)aniline
https://huagongshe.com/reaction/29880
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Fluorophenol | HCID 9732 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Bromoaniline | HCID 11562 | — |
| Catalyst | Copper oxide | HCID 14829 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 3-(4-Fluorophenoxy)aniline | HCID 23506015 | — |
Reaction Steps
In a dry microwave vessel with stir bar, 3-bromoaniline (316 μL, 0.029 mol) and 4-flourophenol (716 mg, 0.064 mol) were added to anhydrous pyridine (10 mL) under nitrogen. To this was added potassium carbonate (1.6 g, 120 mol) and copper(II) oxide (1.2 g, 145 mol). The microwave vessel was sealed then heated in the microwave at normal absorbance at 210° C. for 40 min. The cooled reaction was filtered through a bed of Celite with ethyl acetate. The filtrate was then washed 3 times with concentrated aqueous NaHSO4 and twice with concentrated aqueous NaCl. The organic layer was then dried over magnesium sulfate, filtered and concentrated. Purification over silica using an eluent of hexane and ethyl acetate with a gradient of 0-23% ethyl acetate over 45 min gave 3-(4-fluoro-phenoxy)-phenylamine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07423043B2 |
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| Source dataset | uspto-grants-2008_09 |
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| ORD ID | ord-09df41b16d864eddaa7380ff6ca4a6ce |
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| Source note | uspto-grants-2008_09 |
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