Back
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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Dihydro-7,8-dimethoxy-2H-3-benzazepin-2-oneHCID 1482373—
ReactantHCID 19803730HCID 19803730—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethyl SulfoxideHCID 679—
SolventEthyl AcetateHCID 8857—
ProductHCID 54168333HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05175157
Source datasetuspto-grants-1992_12
ORD IDord-34c9f8524f4744689cf45beb62c38603
Source noteuspto-grants-1992_12