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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2262900Generated: October 25, 2026

tert-Butyl piperazine-1-carboxylate → Tert-butyl 4-(4-phenyl-1,3-oxazol-2-yl)piperazine-1-carboxylate

https://huagongshe.com/reaction/2262900

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
Reactant2-Chloro-4-phenyloxazoleHCID 21408261—
SolventO-XyleneHCID 7237—
ProductTert-butyl 4-(4-phenyl-1,3-oxazol-2-yl)piperazine-1-carboxylateHCID 6877743136.4%

Reaction Steps

A solution of tert-butyl piperazine-1-carboxylate (1.21 g, 6.51 mmol) and 2-chloro-4-phenyl-1,3-oxazole (390 mg, 2.17 mmol) in xylene (50 ml) was stirred at 155° C. for 12 hours. The solvent was distilled off under reduced pressure. The residue was poured to water, and extracted with ethyl acetate. The extract was washed with water and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (hexane: ethyl acetate=9:1) to give 260 mg (12.1%) of the desired product as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07851473B2
Source datasetuspto-grants-2010_12
ORD IDord-d91c89dc96ec4f1cbb566ba1612b675f
Source noteuspto-grants-2010_12