HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 897480Generated: October 30, 2026
4-Bromophenol → 4-(4-Bromophenoxy)benzonitrile
https://huagongshe.com/reaction/897480
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Bromophenol | HCID 7808 | — |
| Reactant | 4-Fluorobenzonitrile | HCID 14517 | — |
| Reactant | 18-Crown-6 | HCID 28557 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-(4-Bromophenoxy)benzonitrile | HCID 22347396 | 51.1% |
Reaction Steps
A mixture of 4-bromophenol (4.56 g, 0.0264 mol), 4-fluorobenzonitrile (0.0264 mol), 18-Crown-6 (0.7 g, 0.00264 mol) and 40% potassium fluoride on alumina (10.8 g) in anhydrous acetonitrile (100 mL) was heated at reflux under an atmosphere of nitrogen for twelve hours. It was cooled to ambient temperature, filtered through a Celite pad and concentrated under reduced pressure. The residue was partitioned between diethyl ether (120 mL) and water (100 mL), the organic phase was further washed with saturated solution of potassium chloride in water, dried with magnesium sulfate and concentrated. The residue was purified by flash chromatography on silica using ethyl acetate/n-heptane (3:97) as mobile phase to yield 4-(4-bromophenoxy)benzonitrile (3.7 g, 0.0135 mol) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06921763B2 |
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| Source dataset | uspto-grants-2005_07 |
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| ORD ID | ord-a42346b2d73849c5b94eed409e61051e |
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| Source note | uspto-grants-2005_07 |
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