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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 586994Generated: October 29, 2026

Ethanol → 7-(4-Propoxyethoxyphenyl)-1-(2-thienylmethyl)-2,3-dihydro-1-benzazepine-4-carboxylic acid

https://huagongshe.com/reaction/586994

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantPotassium CarbonateHCID 11430—
Reactant7-Bromo-1-(2-thienylmethyl)-2,3-dihydro-1-benzazepine-4-carboxylic acidHCID 22329060—
Reactant4-(2-Propoxyethoxy)phenyl borateHCID 86756814—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product7-(4-Propoxyethoxyphenyl)-1-(2-thienylmethyl)-2,3-dihydro-1-benzazepine-4-carboxylic acidHCID 6974932942.3%

Reaction Conditions

Temperature100 °C

Reaction Steps

In toluene (30 ml), ethanol (3 ml) and water (3 ml) were suspended 7-bromo-1-(2-thienylmethyl)-2,3-dihydro-1-benzazepine-4-carboxylic acid (500 mg), 4-propoxyethoxyphenyl borate (615 mg) and potassium carbonate (949 mg), and the suspension was stirred under argon atmosphere for 30 minutes. Then, to the suspension was added tetrakistriphenylphosphinepalladium (111 mg), and the mixture was heated under argon atmosphere at 100° C. for 6 hours. After allowing to cool, water was added thereto, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine and dried with magnesium sulfate. The solvent was evaporated under reduced pressure and the resulting residue was purified with silica gel column chromatography (hexane:ethyl acetate=1:1), which was recrystallized from hexane-ethyl acetate to give 7-(4-propoxyethoxyphenyl)-1-(2-thienylmethyl)-2,3-dihydro-1-benzazepine-4-carboxylic acid (269 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06936602B1
Source datasetuspto-grants-2005_08
ORD IDord-c44ae802cc634eeab57d7d28da3b4839
Source noteuspto-grants-2005_08