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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 26431Generated: October 29, 2026

3-(2-methoxyiminopropyl)-4-(4-methoxyphenyl)-1,5,6,7-tetrahydro-2H-azepinone → HCID 20332954, compound

https://huagongshe.com/reaction/26431

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(2-methoxyiminopropyl)-4-(4-methoxyphenyl)-1,5,6,7-tetrahydro-2H-azepinoneHCID 86736471—
ReactantHCID 178418361HCID 178418361—
CatalystNickelHCID 935—
SolventEthanolHCID 702—
ProductHCID 20332954HCID 20332954—

Reaction Steps

The solution of 6.5 g of 3-(2-methoxyiminopropyl)-4-(4-methoxyphenyl)-1,5,6,7-tetrahydro-2H-azepinone in 150 ml of ethanol is hydrogenated at room temperature and atmospheric pressure in the presence of 10 g of Raney nickel until the uptake of 2 mole equivalents of hydrogen is complete. The mixture is filtered, the filtrate evaporated and the residue dissolved in 100 ml of water and 10 ml of 6 N hydrochloric acid. The acidic solution is washed with diethyl ether, filtered, basified with 30 ml of 3 N aqueous sodium hydroxide and repeatedly extracted with chloroform. The extract is dried, evaporated and the residue is purified by suspension in diethyl ether, to give the 3-(2-aminopropyl)-4-(4-methoxyphenyl)-1,5,6,7-tetrahydro-2H-azepinone melting at 131°-133°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04150129
Source datasetuspto-grants-1979_04
ORD IDord-b22b5f316c484a7f9559a49fc4cf3e77
Source noteuspto-grants-1979_04