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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 586835Generated: October 26, 2026

Water → HCID 22328968, compound

https://huagongshe.com/reaction/586835

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactantmethyl 7-bromo-1-formyl-2,3-dihydro-1H-1-benzazepine-4-carboxylateHCID 22329262—
ReactantHCID 86756179HCID 86756179—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
ProductHCID 22328968HCID 2232896882%

Reaction Steps

To a mixture of methyl 7-bromo-1-formyl-2,3-dihydro-1H-1-benzazepine-4-carboxylate (3.51 g), 4-morpholinophenyl borate (3.51 g) and potassium carbonate (3.75 g) was added a mixture of water (20 ml), ethanol (20 ml) and toluene (100 ml), and the mixture was stirred under argon atmosphere at room temperature for 40 minutes. To the mixture was added tetrakis(triphenylphosphine)palladium (0.52 g), and the mixture was refluxed under argon atmosphere for 12 hours and extracted with ethyl acetate. The organic layer was washed with water and saturated brine, and dried with anhydrous magnesium sulfate. The solvent was evaporated, and the residue was purified with silica gel column chromatography (ethyl acetate/hexane) to give methyl 1-formyl-7-(4-morpholinophenyl)-2,3-dihydro-1H-1-benzazepine-4-carboxylate (3.64 g) as pale yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06936602B1
Source datasetuspto-grants-2005_08
ORD IDord-07f3441d2ee3416e9677d185cb5601e9
Source noteuspto-grants-2005_08