HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 907603Generated: November 1, 2026
4-Fluorophenol → Ethyl difluoro(4-fluorophenoxy)acetate
https://huagongshe.com/reaction/907603
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Fluorophenol | HCID 9732 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ethyl bromodifluoroacetate | HCID 69585 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Ethyl difluoro(4-fluorophenoxy)acetate | HCID 53436401 | 59% |
Reaction Steps
A suspension of 60% of NaH in oil (3.84 g, 96 mmol) was washed three times with hexanes and the solid was suspended in dry DMF (80 ml). 4-Fluorophenol (8.96 g, 80 mmol) was slowly added over a period of 5 min and the reaction mixture was stirred at rt for about 10 min. The reaction mixture was cooled at 0° C. and 2-bromo-2,2-difluoroacetic acid ethyl ester (16.24 g, 80 mmol) was slowly added. The reaction mixture was heated at 90° C. for 20 h. After allowing the reaction to reach room temperature, ethyl ether (300 ml) was added and the suspension was washed with water and brine. After drying the organic layer over sodium sulfate for 15 min, the solvent was evaporated and the crude was purified by flash chromatography, using a mixture of ethyl acetate/hexanes (1/10) to give 2,2-difluoro-2-(4-fluorophenoxy)acetic acid ethyl ester as an oil (11.0 g, 59%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08013186B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-22b73e74ccca480e8dc12fc16cddffce |
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| Source note | uspto-grants-2011_09 |
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