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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1263475Generated: November 1, 2026

Piperazine → HCID 22313131, compound

https://huagongshe.com/reaction/1263475

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
Reactant4-Fluorobenzyl chlorideHCID 9602—
ReactantPiperazine-hydrogen chloride-water (1:2:1)HCID 12197850—
SolventEthanolHCID 702—
ProductHCID 22313131HCID 2231313191%

Reaction Conditions

Temperature65 °C

Reaction Steps

A solution of 2.154 g(25 mM) of piperazine in 25 mL of absolute ethanol, was warmed in a bath at 65° C. Piperazine dihydrochloride hydrate (3.9765 g(25 mM)) was dissolved in the solution, by swirling. In the bath at 65° C. 3.6145 g(25 mM) of 4-fluorobenzyl chloride was added to the solution with vigorous stirring. The separation of white needles commenced almost immediately. After the solution had been stirred for an additional 25 minutes at 65° C., it was cooled, and the unstirred solution was kept in an ice bath for about 30 minutes. The crystals of piperazine dihydrochloride hydrate were collected by suction filtration, washed with three 5 mL portions of ice-cold absolute ethanol, and then dried. Approximately 3.989g(100.3%) of the dihydrochloride was recovered. Filtrate from this solution was evaporated to dryness at reduced pressure and crude 1-(4-methoxybenzyl)-4-piperazinium chloride was left as a residue. For removal of any piperazine dihydrochloride, the chloride may be crystallized after rapidly filtering a hot solution in about 20 mL of absolute ethanol. Concentration of the filtrate followed by cooling gave 5.248 g(91%) of 1-(4-fluorobenzyl)-4-piperazinium chloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06541479B1
Source datasetuspto-grants-2003_04
ORD IDord-32f6f3c44edf4c4ebc91ecb2dd9b15ac
Source noteuspto-grants-2003_04