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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1533869Generated: October 26, 2026

Hydrochloric Acid → 3-(4-Methyl-1-piperazinyl)propoxyamine trihydrochloride

https://huagongshe.com/reaction/1533869

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantN-[3-(4-Methyl-1-piperazinyl)propoxy]phthalimideHCID 19911312—
SolventEthanolHCID 702—
Product3-(4-Methyl-1-piperazinyl)propoxyamine trihydrochlorideHCID 19911349—

Reaction Conditions

Temperature20 °C

Reaction Steps

3-(4-Methyl-1-piperazinyl)propoxyamine trihydrochloride may be obtained in the following manner: a solution of N-[3-(4-methyl-1-piperazinyl)propoxy]phthalimide (5.7 g) in 6 N hydrochloric acid (30 cc) is heated to reflux for 3 hours. After 18 hours' stirring at a temperature in the region of 20° C., the suspension obtained is filtered and the filtrate is concentrated to dryness under reduced pressure (20 mm Hg; 2.7 kPa) at a temperature in the region of 60° C. A crude product (6 g) is thereby obtained, which is resuspended in ethanol (30 cc). The crystals which appear are separated by filtration, washed 3 times with ethanol (45 cc in total) and then 3 times with ethyl ether (75 cc in total) and finally dried under reduced pressure (20 mm Hg; 2.7 kPa) at a temperature in the region of 20° C. 3-(4-Methyl-1-piperazinyl)propoxyamine trihydrochloride (3.4 g) is thereby obtained in the form of cream-coloured crystals, m.p. 240° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05086051
Source datasetuspto-grants-1992_02
ORD IDord-6c43abffdf344be597eeecb1d6dd27d9
Source noteuspto-grants-1992_02