HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1681999Generated: November 1, 2026
1,3-Dihydro-7,8-dimethoxy-2H-3-benzazepin-2-one → HCID 54168333, compound
https://huagongshe.com/reaction/1681999
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,3-Dihydro-7,8-dimethoxy-2H-3-benzazepin-2-one | HCID 1482373 | — |
| Reactant | HCID 19803730 | HCID 19803730 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 54168333 | HCID 54168333 | — |
Reaction Steps
2.3 g (0.02 mol) of potassium tert.butoxide are added to a solution of 4.4 g (0.02 mol) of 7,8-dimethoxy-1,3-dihydro-2H-3-benzazepin-2-one in 100ml of absolute dimethylsulphoxide. After stirring for 30 minutes at ambient temperature, 5.6 g (0.020 mol) of 1-benzyl-3-bromomethyl-hexahydro-azepine are added and the resulting mixture is stirred for 2 hours at ambient temperature. The reaction mixture is dissolved in ethyl acetate and extracted several times with water. The organic phase is dried over magnesium sulphate and evaporated down in vacuo. The residue is purified by column chromatography over aluminium oxide N (activity II, eluant: methylene chloride, methylene chloride+0.3% ethanol). Yield: 4.2 g (50% of theory), IR spectrum (methylene chloride): 1655 cm-1 (CO).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05175157 |
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| Source dataset | uspto-grants-1992_12 |
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| ORD ID | ord-34c9f8524f4744689cf45beb62c38603 |
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| Source note | uspto-grants-1992_12 |
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