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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 566005Generated: October 29, 2026

Potassium Carbonate → Ethyl 7-(4-chlorophenyl)-2,3-dihydro-1-benzoxepine-4-carboxylate

https://huagongshe.com/reaction/566005

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 10709089HCID 10709089—
Reactant4-Chlorophenyl borateHCID 86756166—
CatalystHCID 178418397HCID 178418397—
SolventToluene-ethanol waterHCID 66602552—
ProductEthyl 7-(4-chlorophenyl)-2,3-dihydro-1-benzoxepine-4-carboxylateHCID 1847221183%

Reaction Steps

Under argon atmosphere, a solution of ethyl 7-bromo-2,3-dihydro-1-benzoxepine-4-carboxylate (500 mg), 4-chloro-phenyl borate (289 mg) and potassium carbonate (464 mg) in toluene-ethanol-water (20-2-2 ml) was stirred at room temperature for 1 hour. To the reaction mixture was added tetrakistriphenyl-phosphinepalladium (0.06 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=1:19) to give ethyl 7-(4-chlorophenyl)-2,3-dihydro-1-benzoxepine-4-carboxylate (459 mg) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06172061B2
Source datasetuspto-grants-2001_01
ORD IDord-7011ec28387c466c91a796faa29b2d39
Source noteuspto-grants-2001_01