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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1706910Generated: October 29, 2026

Water → 3-(2-pyrrolidinopropyl)-4-(3-methoxyphenyl)-1,5,6,7-tetrahydro-2H-azepinone

https://huagongshe.com/reaction/1706910

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPyrrolidineHCID 31268—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
Reactant3-acetonyl-4-(3-methoxyphenyl)-1,5,6,7-tetrahydro-2H-azepinoneHCID 20332934—
SolventBenzeneHCID 241—
Product3-(2-pyrrolidinopropyl)-4-(3-methoxyphenyl)-1,5,6,7-tetrahydro-2H-azepinoneHCID 20332936—

Reaction Steps

The solution of 1.36 g of 3-acetonyl-4-(3-methoxyphenyl)-1,5,6,7-tetrahydro-2H-azepinone, 0.52 g of pyrrolidine and 0.1 g of p-toluenesulfonic acid hydrate in 10 ml of benzene is refluxed with water separation for 4 hours and evaporated. The residue is dissolved in 15 ml of ethanol and the solution hydrogenated over 0.1 g of platinum oxide at atmospheric pressure and room temperature. The mixture is filtered, the filtrate evaporated and the resulting oil dissolved in 2 N hydrochloric acid. The solution is washed with benzene, basified with 3 N aqueous sodium hydroxide and extracted with diethyl ether. The extract is dried, evaporated and the residue recrystallized from petroleum ether and hexane, to yield the 3-(2-pyrrolidinopropyl)-4-(3-methoxyphenyl)-1,5,6,7-tetrahydro-2H-azepinone melting at 94° to 96°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04209514
Source datasetuspto-grants-1980_06
ORD IDord-79e1020a9f72431993745dc4f64bd94d
Source noteuspto-grants-1980_06