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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1672186Generated: October 31, 2026

Ethyl Acetate → 8-methyl-3,4-dihydro-1H-1-benzazepine-2,5-dione

https://huagongshe.com/reaction/1672186

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantTetramethyltinHCID 11661—
ReactantPotassium FluorideHCID 522689—
Reactant8-iodo-2,3,4,5-tetrahydro-1H-1-benzazepine-2,5-dioneHCID 58476623—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418397HCID 178418397—
SolventDimethylformamideHCID 6228—
Product8-methyl-3,4-dihydro-1H-1-benzazepine-2,5-dioneHCID 5847663932%

Reaction Conditions

Temperature120 °C

Reaction Steps

To a degassed solution of 8-iodo-3,4-dihydro-1H-1-benzazepine-2,5-dione (0.3 g, 1.0 mmol) in DMF (5 mL) was added CuI (19 mg, 0.1 mmol), KF (116 mg, 2.0 mmol), Me4Sn (0.28 mL, 2.0 mmol), and Pd(PPh3)4 (116 mg, 0.1 mmol). The reaction mixture was allowed to stir at 120° C. for 4 h. After being allowed to cool to rt, EtOAc (50 mL) and a 1M aqueous KF solution (25 mL) were added and the solution was allowed to stir for an additional 40 min. The mixture was filtered over Celite®. The organic solution was separated, washed with brine, dried over Na2SO4, filtered and concentrated. The residue was purified by column chromatography to provide 8-methyl-3,4-dihydro-1H-1-benzazepine-2,5-dione (60 mg, 32%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07998952B2
Source datasetuspto-grants-2011_08
ORD IDord-e29509e6e1aa46a5abcb77cb3896757a
Source noteuspto-grants-2011_08