HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 389986Generated: October 28, 2026
Potassium Hydroxide → 4-(4-Ethyl-5-fluoro-2-methoxyphenoxy)-3-fluorobenzonitrile
https://huagongshe.com/reaction/389986
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 | — |
| Solvent | Pentane | HCID 8003 | — |
| Product | 4-(4-Ethyl-5-fluoro-2-methoxyphenoxy)-3-fluorobenzonitrile | HCID 51034749 | — |
Reaction Steps
Potassium hydroxide (2.4 g, 43.13 mmol) was added to a solution of 4-ethyl-5-fluoro-2-methoxyphenol (6.1 g, 35.94 mmol) and 3,4-difluorobenzonitrile (5.0 g, 35.94 mmol) in anhydrous acetonitrile (80 mL). The reaction mixture was stirred at 85° C. overnight then concentrated under vacuum. The residue was solubilized in ethyl acetate (300 mL) and diluted by addition of a saturated solution of ammonium chloride (200 mL). The aqueous layer was separated and extracted with ethyl acetate (2×200 mL). The combined organic phases were dried over sodium sulfate, filtered and concentrated to dryness to give a brown solid. After trituration in pentane, the title product was obtained as a brown solid (8.10 g, 77%).
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-d8048e8fa2184f09a9cde050ab68251f |
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| Source note | uspto-grants-2013_02 |
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