HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1694879Generated: October 31, 2026
tert-Butyl hydroperoxide → 4-Oxiranecarbonyl piperazine-1-carboxylic acid tert butyl ester
https://huagongshe.com/reaction/1694879
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butyl hydroperoxide | HCID 6410 | — |
| Reactant | Sodium Sulfite | HCID 24437 | — |
| Reactant | tert-Butyl 4-acryloylpiperazine-1-carboxylate | HCID 58593060 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Oxiranecarbonyl piperazine-1-carboxylic acid tert butyl ester | HCID 86701126 | 19.9% |
Reaction Steps
A solution of anhydrous t-butyl hydroperoxide (5.5M in nonane, 2.07 ml, 11.38 mmol, 1.5 eq) was added to anhydrous THF (50 mL), at −78° C. under argon. To the resulting solution at −78° C. was added butyl lithium (2.3M in n-hexane, 3.36 ml, 8.4 mmol, 1.1 eq) was added and the solution is stirred for a further 5 min at this temperature. A solution of the 4-Acryloyl-piperazine-1-carboxylic acid tert butyl ester (1.96 g, 7.64 mmol, 1 eq) in anhydrous THF (20 ml) was then added dropwise at −78° C. The resulting mixture was then allowed to warm slowly to room temperature and stirred for a further 16 hr. To the mixture was then added sodium sulfite (1.5 g, 12 mmol, 1.55 eq) and this was then stirred for 15 min. The mixture was then diluted with diethylether (50 ml), filtered through celite and the filtrate evaporated. The residue was purified by chromatography (ethyl acetate/n-hexane 4/1) to give the product (0.39 g, 19%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08158797B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-ef6704291b3f4c789480f290dcf64860 |
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| Source note | uspto-grants-2012_04 |
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