Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 27087Generated: October 25, 2026

Piperazine → 1-(Piperazin-1-yl)propan-1-one hydrochloride

https://huagongshe.com/reaction/27087

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
ReactantPropionamideHCID 6578—
Reactant4-Propanoylpiperazine-1-carbonyl chlorideHCID 14369520—
CatalystIodineHCID 807—
SolventO-XyleneHCID 7237—
Product1-(Piperazin-1-yl)propan-1-one hydrochlorideHCID 13017829—

Reaction Steps

The 1-chlorocarbonyl-4-propionylpiperazine used as starting material can be prepared as follows. Anhydrous piperazine (120 g.) and propionamide (m.p. 80° C., 102 g.) in anhydrous xylene (100 cm3) are heated under reflux for 48 hours in the presence of iodine (0.9 g.) to give 1-propionylpiperazine hydrochloride (153.0 g.), m.p. 165° C. 1-Propionylpiperazine is liberated from its hydrochloride by the action of an excess of ammonia in diethyl ether. The ammonium chloride formed is separated by filtration and the 1-propionylpiperazine is isolated by evaporation of the ether.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04220646
Source datasetuspto-grants-1980_09
ORD IDord-18f5dfb69f5b4bd8898f781342fac926
Source noteuspto-grants-1980_09