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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2364705Generated: October 30, 2026

tert-Butyl piperazine-1-carboxylate → (S)-1-Boc-4-(oxiran-2-ylmethyl)piperazine

https://huagongshe.com/reaction/2364705

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
Reactant(+)-EpichlorohydrinHCID 149428—
SolventEthanolHCID 702—
Product(S)-1-Boc-4-(oxiran-2-ylmethyl)piperazineHCID 1097762695%

Reaction Steps

Tert-butyl piperazine-1-carboxylate 7a (7.44 g, 40 mmol) and (S)-2-chloromethyl-oxirane (3.70 g, 40 mmol) were dissolved in 60 mL of ethanol. The reaction solution was stirred for 12 hours. The resulting solution was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography to obtain the title compound tert-butyl 4-[[(2S)-oxiran-2-yl]methyl]piperazine-1-carboxylate 20a (9.20 g, yield: 95.0%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691822B2
Source datasetuspto-grants-2014_04
ORD IDord-82a0d23784844d8f9eee4f4ee52d0d3a
Source noteuspto-grants-2014_04