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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2052806Generated: November 2, 2026

Piperazine → Piperazine, 1-(phenylmethyl)-, hydrochloride (1:2)

https://huagongshe.com/reaction/2052806

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
ReactantBenzyl ChlorideHCID 7503—
ReactantPotassium HydroxideHCID 14797—
CatalystHexadecyltrimethylammonium BromideHCID 5974—
SolventBenzeneHCID 241—
SolventWaterHCID 962—
ProductPiperazine, 1-(phenylmethyl)-, hydrochloride (1:2)HCID 1219804655%

Reaction Steps

A mixture of piperazine (350 mmol), KOH (100 mmol) and hexadecyl-trimethyl ammonium bromide (CTAB, 1 mmol) in water (18 ml) was heated to get a solution. Thereafter, benzyl chloride (100 mmol) in 140 ml of benzene was added to the solution dropwise at 70° C., and refluxed for 1 h. The organic layer was washed with water and saline, dried (MgSO4), filtered and evaporated, the residue was dissolved by 50 ml of ethanol and adjusted to a PH of 2 by HCl/C2H5OH (5N), the resulting precipitate was recrystallized from ethanol to obtain N-benzyl piperazine dihydrochloride (55-86%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07326710B2
Source datasetuspto-grants-2008_02
ORD IDord-3683190dea0e4fcfb9ee16547cfc9322
Source noteuspto-grants-2008_02