HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 389979Generated: October 30, 2026
Potassium Hydroxide → 4-(4-Ethyl-5-fluoro-2-methoxyphenoxy)-3-fluorobenzonitrile
https://huagongshe.com/reaction/389979
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 3,4-Difluorobenzonitrile | HCID 587203 | — |
| Reactant | 4-Ethyl-5-fluoro-2-methoxyphenol | HCID 45933640 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-(4-Ethyl-5-fluoro-2-methoxyphenoxy)-3-fluorobenzonitrile | HCID 51034749 | 94.2% |
Reaction Steps
A suspension of 4-ethyl-5-fluoro-2-methoxyphenol (1 g, 5.87 mmol), 3,4-difluorobenzonitrile (899 mg, 6.46 mmol) and potassium hydroxide (395 mg, 7.04 mmol) in anhydrous acetonitrile (35 mL) under argon was stirred at 80° C. overnight. The reaction mixture was concentrated under vacuum and diluted with ethyl acetate and a saturated aqueous solution of ammonium chloride. The aqueous layer was separated and extracted twice with ethyl acetate. The combined organic phases were dried over sodium sulfate, filtrated and concentrated in vacuo to give a brown oil (1.6 g). The crude product was purified by flash chromatography on silica gel, using cyclohexane/ethyl acetate (9:1) as eluent. The title product was obtained as a colourless oil that crystallized slowly (1.42 g, 84%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08383621B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-c6f60e1e656e4b88b6db5bd14cf6ab3e |
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| Source note | uspto-grants-2013_02 |
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