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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1769685Generated: October 31, 2026

Piperazine → N-(4,5-diphenyloxazolyl)methyl piperazine

https://huagongshe.com/reaction/1769685

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
Reactant2-Bromomethyl-4,5-diphenyl-oxazoleHCID 568599—
SolventEthanolHCID 702—
ProductN-(4,5-diphenyloxazolyl)methyl piperazineHCID 21443198.4%

Reaction Steps

A mixture of 4,5-diphenyl-2-bromomethyloxazole (X; 20 g, 0.063 moles) and excess piperazine (10 mol equivalent) in 400 ml of absolute ethanol was stirred overnight at room temperature. The reaction mixture was evaporated and the residue was taken up in 4X200 ml of methylene chloride and washed several times with water and brine. The organic layer was dried over Na2SO4, evaporated and the product was obtained as a yellow solid (19.8 g, 95%) after passing through a silica gel column and eluting with a mixture of methanol/chloroform (1:9). This procedure is amenable for large scale synthesis. MS (DCl) MH+ 320.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05382584
Source datasetuspto-grants-1995_01
ORD IDord-d96bb9843a674c42b9691b288054e724
Source noteuspto-grants-1995_01