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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1888877Generated: November 2, 2026

tert-Butyl hydroperoxide → 4-Oxiranecarbonyl piperazine-1-carboxylic acid tert butyl ester

https://huagongshe.com/reaction/1888877

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl hydroperoxideHCID 6410—
ReactantSodium SulfiteHCID 24437—
Reactanttert-Butyl 4-acryloylpiperazine-1-carboxylateHCID 58593060—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product4-Oxiranecarbonyl piperazine-1-carboxylic acid tert butyl esterHCID 8670112619.9%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501774B2
Source datasetuspto-grants-2013_08
ORD IDord-6ce4041c2a314719bd07642da57d7eba
Source noteuspto-grants-2013_08