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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2293990Generated: November 1, 2026

Piperazine → 2-(Piperazin-1-yl)-1,3-benzoxazole

https://huagongshe.com/reaction/2293990

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
Reactant2-ChlorobenzoxazoleHCID 11986—
SolventAcetonitrileHCID 6342—
Product2-(Piperazin-1-yl)-1,3-benzoxazoleHCID 64781857.1%

Reaction Steps

In 200 ml of acetonitrile were dissolved 33.6 g (0.39 mole) of piperazine and 10.0 g (0.065 mole) of 2-chlorobenzoxazole, and 9.0 g (0.065 mole) of potassium carbonate and a catalytic amount of potassium iodide were added thereto. The mixture was refluxed by heating for 11 hours under stirring. The mixture was cooled to room temperature and then filtered. The filtrate was concentrated under reduced pressure, and the residue was applied to silica gel column chromatography (the eluent used was a mixture of chloroform:methanol=9:1) to obtain 7.54 g of 1-(2-benzoxazolyl)piperazine as white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05688791
Source datasetuspto-grants-1997_11
ORD IDord-e886c5a785014f8aadb7e9d33861b694
Source noteuspto-grants-1997_11