HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 65592Generated: October 25, 2026
2-Fluorophenol → 2-[4-(2-Fluorophenoxy)phenyl]propionic acid
https://huagongshe.com/reaction/65592
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Fluorophenol | HCID 9707 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2-(4-Iodophenyl)propanoic acid | HCID 15225573 | — |
| Catalyst | Water | HCID 962 | — |
| Catalyst | Copper | HCID 23978 | — |
| Product | 2-[4-(2-Fluorophenoxy)phenyl]propionic acid | HCID 20559786 | — |
Reaction Steps
2-Fluorophenol (2.35 g.) was fused with potassium hydroxide (1.7 g.) and a few drops of water by heating to 180° C. 2-(4-Iodophenyl)propionic acid (2.76 g.) and copper powder (0.1 g.) were then added and the melt ws heated at 160°-170° C. for 1 hour. The cooled solid was partitioned with methylene chloride (50 ml.) and 2.5N sodium hydroxide (50 ml.). The aqueous layer was acidified with hydrochloric acid, the resulting gum was extracted into ether, and the ether extract was extracted with saturated potassium carbonate solution. This aqueous extract was acidified with hydrochloric acid and the product isolated in ether. After evaporation the resulting solid was purified by preparative layer chromatography using 5% acetic acid/petroleum ether b.p. 62°-68° C. and eluting with ethyl acetate. Recrystallization from petroleum ether b.p. 62°-68° C. gave 2-[4-(2-fluorophenoxy)phenyl]propionic acid, m.p. 106°-108° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04128573 |
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| Source dataset | uspto-grants-1978_12 |
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| ORD ID | ord-a480ab6c73eb43689a2bfa1d299ef1ed |
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| Source note | uspto-grants-1978_12 |
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