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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2387976Generated: October 30, 2026

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

https://huagongshe.com/reaction/2387976

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantTributylvinyltinHCID 81998—
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-vinyl-3,4-dihydro-1H-1-benzazepine-2,5-dioneHCID 6733659740%

Reaction Conditions

Temperature100 °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), tributylethenylstannane (0.58 mL, 2.0 mmol), and Pd(PPh3)4 (116 mg, 0.1 mmol). The reaction mixture was allowed to stir at 100° 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 mixture was allowed to stir for an additional 40 min. The mixture was filtered over Celite® and the organic solution was separated, washed with brine, dried over Na2SO4, filtered and concentrated. The residue was treated with n-pentane and filtered. The resulting solid was purified by column chromatography to provide 8-vinyl-3,4-dihydro-1H-1-benzazepine-2,5-dione (80 mg, 40%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08268992B2
Source datasetuspto-grants-2012_09
ORD IDord-9330e24832ce4a0482c1bcb12d3b7433
Source noteuspto-grants-2012_09