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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 586924Generated: October 30, 2026

Ethanol → methyl 1-benzyl-7-[4-(2-propoxyethoxy)phenyl]-2,3-dihydro-1H-1-benzazepine-4-carboxylate

https://huagongshe.com/reaction/586924

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantPotassium CarbonateHCID 11430—
Reactantmethyl 1-benzyl-7-bromo-2,3-dihydro-1H-1-benzazepine-4-carboxylateHCID 22329080—
Reactant4-(2-Propoxyethoxy)phenyl borateHCID 86756814—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
Productmethyl 1-benzyl-7-[4-(2-propoxyethoxy)phenyl]-2,3-dihydro-1H-1-benzazepine-4-carboxylateHCID 2232889871%

Reaction Steps

A mixture of methyl 1-benzyl-7-bromo-2,3-dihydro-1H-1-benzazepine-4-carboxylate (0.3 g), 4-(2-propoxyethoxy)phenyl borate (0.24 g), 1M potassium carbonate solution (2.5 ml), ethanol (2.5 ml) and toluene (25 ml) was stirred under argon atmosphere at room temperature for 30 minutes. To the mixture was added tetrakis(triphenylphosphine)palladium (0.04 g), and the mixture was refluxed under argon atmosphere overnight. The mixture was extracted with ethyl acetate, and the organic layer was washed with water and saturated brine and dried with anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure and the residue was purified with silica gel column chromatography (ethyl acetate/hexane) to give methyl 1-benzyl-7-[4-(2-propoxyethoxy)phenyl]-2,3-dihydro-1H-1-benzazepine-4-carboxylate (0.27 g) as yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06936602B1
Source datasetuspto-grants-2005_08
ORD IDord-b0302f80ae4a441489c35a1b53f13464
Source noteuspto-grants-2005_08