HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2286681Generated: October 26, 2026
Potassium Carbonate → 4-[4-(4-Trifluoromethylphenoxy)phenoxy]-2-pentenoic acid
https://huagongshe.com/reaction/2286681
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | p-(4-(Trifluoromethyl)phenoxy)phenol | HCID 170230 | — |
| Reactant | 3,4-Dibromopentanoic acid | HCID 15089970 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-[4-(4-Trifluoromethylphenoxy)phenoxy]-2-pentenoic acid | HCID 157794 | 75% |
Reaction Steps
In a reactor, 30 g of tetrahydrofuran was charged and 12.7 g (0.05 mole) of 4-(4-trifluoromethylphenoxy)phenol, 14.3 g (0.055 mole) of 3,4-dibromopentanoic acid and 16.6 g of potassium carbonate were charged. They were refluxed for 6 hours to react them. After the reaction, tetrahydrofurane was distilled off from the reaction mixture and then 50 ml of chlorobenzene was added to the resulting mixture and then conc. hydrochloric acid was added to the resulting mixture with stirring to be acidic and then, the water phase was separated and the organic phase washed with water and then, chlorobenzene and low boiling by-products were distilled off at 100° C. under a reduced pressure (0.02-0.05 mmHg) to obtain 13.2 g of 4-[4-(4-trifluoromethylphenoxy)phenoxy]-2-pentenoic acid. (nD20 1.5284). The yield was 75%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04267317 |
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| Source dataset | uspto-grants-1981_05 |
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| ORD ID | ord-ef870c34523649ba94b5e2223d72929e |
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| Source note | uspto-grants-1981_05 |
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