HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1277181Generated: October 29, 2026
Potassium Carbonate → Ethyl 7-(4-trifluoromethylphenyl)-2,3-dihydro-1-benzoxepine-4-carboxylate
https://huagongshe.com/reaction/1277181
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 10709089 | HCID 10709089 | — |
| Reactant | 4-Trifluoromethylphenyl borate | HCID 86756167 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Toluene-ethanol water | HCID 66602552 | — |
| Product | Ethyl 7-(4-trifluoromethylphenyl)-2,3-dihydro-1-benzoxepine-4-carboxylate | HCID 10808612 | 80.2% |
Reaction Steps
Under argon atmosphere, a solution of ethyl 7-bromo-2,3-dihydro-1-benzoxepine-4-carboxylate (500 mg), 4-trifluoromethylphenyl borate (351.5 mg) and potassium carbonate (0.47 g) in toluene-ethanol-water (20-2-2 ml) was stirred at room temperature for 1 hour. To the reaction mixture was added tetrakistriphenylphosphinepalladium (0.06 g), and the mixture was refluxed for 20 hours and cooled to room temperature. The organic layer was washed with saturated sodium chloride solution, dried with magnesium sulfate and concentrated under reduced pressure. The residue was separated and purified with column chromatography (ethyl acetate/hexane=1:10) to give ethyl 7-(4-trifluoromethylphenyl)-2,3-dihydro-1-benzoxepine-4-carboxylate (489 mg) as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06166006 |
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| Source dataset | uspto-grants-2000_12 |
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| ORD ID | ord-4b72248b4b324d41813752bad3ce8d9f |
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| Source note | uspto-grants-2000_12 |
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