HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1892173Generated: November 1, 2026
Ethyl Acetate → 8-methyl-3,4-dihydro-1H-1-benzazepine-2,5-dione
https://huagongshe.com/reaction/1892173
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Tetramethyltin | HCID 11661 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | 8-iodo-2,3,4,5-tetrahydro-1H-1-benzazepine-2,5-dione | HCID 58476623 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 8-methyl-3,4-dihydro-1H-1-benzazepine-2,5-dione | HCID 58476639 | 32% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08507667B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-44af539fa903422d97ba1b52e5359b60 |
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| Source note | uspto-grants-2013_08 |
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