HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2228224Generated: November 1, 2026
Potassium Carbonate → Ethyl 7-(4-methylthiophenyl)-2,3-dihydro-1-benzoxepine-4-carboxylate
https://huagongshe.com/reaction/2228224
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 10709089 | HCID 10709089 | — |
| Reactant | Toluene-ethanol water | HCID 66602552 | — |
| Reactant | 4-Methyl-thiophenyl borate | HCID 86756174 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Product | Ethyl 7-(4-methylthiophenyl)-2,3-dihydro-1-benzoxepine-4-carboxylate | HCID 18472190 | — |
Reaction Steps
Under argon atmosphere, a solution of ethyl 7-bromo-2,3-dihydro-1-benzoxepine-4-carboxylate (1.0 g), 4-methyl-thiophenyl borate (622 mg) and potassium carbonate (0.93 g) in toluene-ethanol-water (30-3-3 ml) was stirred at room temperature for 1 hour. To the reaction mixture was added tetrakistriphenyl-phosphinepalladium (117 mg), and the mixture was refluxed for 16 hours. To the reaction mixture was added tetrakistriphenyl-phosphinepalladium (0.13 g), and the mixture was refluxed for 24 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-methylthio-phenyl)-2,3-dihydro-1-benzoxepine-4-carboxylate (442 mg) as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06413947B1 |
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| Source dataset | uspto-grants-2002_07 |
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| ORD ID | ord-c407a16fb19044d0ad5064b89c279149 |
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| Source note | uspto-grants-2002_07 |
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