HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1767417Generated: October 31, 2026
Ethyl bromoacetate → 4-Cyano-3-fluorophenoxyacetic acid
https://huagongshe.com/reaction/1767417
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Fluoro-4-hydroxybenzonitrile | HCID 2734675 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 4-Cyano-3-fluorophenoxyacetic acid | HCID 22610158 | 65.4% |
Reaction Steps
The mixture of 2-fluoro-4-hydroxybenzonitrile (274 mg, 2.1 mmol), potassium carbonate (910 mg, 6.6 mmol), ethyl bromoacetate (500 mg, 3.0 mmol) and acetone (25 ml) was refluxed for 6 h. After cooling, the mixture was filtered to remove potassium carbonate. The filtrate was concentrated under reduced pressure. To this residue, 10 ml dioxane and 14 ml 5% sodium hydroxide solution were added. After the mixture was stirred at room temperature overnight, it was acidified with concentrated hydrochloric acid to pH 1, and then extracted three times with ethyl acetate (20 ml each). Organic phases were combined, washed with water and brine, dried over magnesium sulfate, filtered, and then evaporated in vacuo. The residue was recrystallized from ethanol and petroleum ether to give 268 mg 4-cyano-3-fluorophenoxyacetic acid as white crystals, mp 150-152° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | USRE039707E1 |
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| Source dataset | uspto-grants-2007_06 |
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| ORD ID | ord-4e9ef3eccce7472b8f6368b0de377b71 |
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| Source note | uspto-grants-2007_06 |
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