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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2294111Generated: October 31, 2026

1-Benzylpiperazine → 4-Benzyl-1-(2-oxazol-2-ylphenyl)piperazine

https://huagongshe.com/reaction/2294111

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-BenzylpiperazineHCID 75994—
Reactant2-(2-Fluorophenyl)oxazoleHCID 10607086—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product4-Benzyl-1-(2-oxazol-2-ylphenyl)piperazineHCID 1056765237.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of N-benzylpiperazine (3.56 g, 20.2 mmol) in 25 mL of THF was cooled to 0° C. and then n-butyllithium was added. The mixture was stirred at 0° C. for 30 minutes and at room temperature for an additional hour. The mixture was cooled to 0° C. and then 2-fluoro-1-oxazol-2-ylbenzene (1.1 g, 6.75 mmol) was slowly added. The mixture was allowed to warm to room temperature and stirred at room temperature for 90 minutes. The mixture was quenched with water and the aqueous layer was separated and extracted with ethyl acetate (3×30 mL). The combined extract was washed with brine, dried (MgSO4) and concentrated. The residue was purified on silica gel by column chromatography eluting with hexanes/ethyl acetate (10:1) to give 4-benzyl-1-(2-oxazol-2-ylphenyl)piperazine (0.805 g, 2.52 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05688795
Source datasetuspto-grants-1997_11
ORD IDord-8558ed40bfb04284812fdd36fb539722
Source noteuspto-grants-1997_11