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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Benzylpiperazine | HCID 75994 | — |
| Reactant | 2-(2-Fluorophenyl)oxazole | HCID 10607086 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Benzyl-1-(2-oxazol-2-ylphenyl)piperazine | HCID 10567652 | 37.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05688795 |
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| Source dataset | uspto-grants-1997_11 |
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| ORD ID | ord-8558ed40bfb04284812fdd36fb539722 |
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| Source note | uspto-grants-1997_11 |
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