HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1581786Generated: November 1, 2026
Potassium Carbonate → HCID 22723462, compound
https://huagongshe.com/reaction/1581786
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Bromothiophene | HCID 13851 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 5-Fluoro-2-methoxyphenylboronic acid | HCID 2782673 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 22723462 | HCID 22723462 | 243.3% |
Reaction Steps
To dioxane (113 ml) is added 2-methoxy-5-fluorophenylboronic acid (4.25 g, 24.9 mmol), 2-bromothiophene (3.65 g, 22.7 mmol, 0.9 eq.) and potassium carbonate (2M, 37 ml). Palladium (0) tetrakistriphenylphoshine (0.03 eq.) is then added and the resulting mixture is heated to 85° C. for 3 hours. The reaction is cooled to room temperature and poured into ethyl acetate and water. The aqueous layer is extracted twice with ethyl acetate. The organic layers are combined, and dried over sodium sulfate, concentrated to a brown oil and the resulting residue is flash chromatographed in 20% toluene/hexanes to afford 11.5 g of 2-(thien-2-yl)-4-fluoroanisole (90%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06730792B2 |
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| Source dataset | uspto-grants-2004_05 |
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| ORD ID | ord-4955e1166cb2461ba7d1c1fbc6bb17ef |
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| Source note | uspto-grants-2004_05 |
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