HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2286435Generated: October 26, 2026
Potassium Carbonate → HCID 54137616, compound
https://huagongshe.com/reaction/2286435
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-(5-Trifluoromethyl-pyridin-2-yloxy)-phenol | HCID 155241 | — |
| Reactant | Methyl 4-bromo-2-pentenoate | HCID 54128087 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | HCID 54137616 | HCID 54137616 | 84% |
Reaction Steps
In 50 ml of methyl ethyl ketone, 2.0 g (0.0078 mole) of 4-[5-(trifluoromethyl)-2-pyridinyloxy]phenol, 3.2 g of methyl 4-bromo-2-pentenoate, and 2.0 g of potassium carbonate were refluxed with constant stirring for 32 hours. Upon cooling to room temperature, the suspension was filtered through celite and the insoluble material washed with 75 ml of acetone. The filtrate was concentrated under reduced pressure to give an oily residue which was dissolved in 125 ml of ethyl ether and transferred to a separatory funnel. After washing with saturated sodium bicarbonate and water, the ether layer was dried over magnesium sulfate and charcoal filtered. Under reduced pressure, the solvent was evaporated and traces of volatile impurities removed at 0.4 mm Hg. (50° for 2 hours) to yield 2.4 g (84% ) of product, ND25 1.520.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04266063 |
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| Source dataset | uspto-grants-1981_05 |
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| ORD ID | ord-08a717429fa74a9b83e31aa43b42dc95 |
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| Source note | uspto-grants-1981_05 |
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