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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2364686Generated: October 30, 2026

tert-Butyl piperazine-1-carboxylate → Tert-butyl 4-[[(2R)-oxiran-2-yl]methyl]piperazine-1-carboxylate

https://huagongshe.com/reaction/2364686

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
Reactant(-)-EpichlorohydrinHCID 2734062—
SolventEthanolHCID 702—
ProductTert-butyl 4-[[(2R)-oxiran-2-yl]methyl]piperazine-1-carboxylateHCID 1101013174%

Reaction Steps

Tert-butyl piperazine-1-carboxylate 7a (3.72 g, 20 mmol) was dissolved in 40 mL of ethanol followed by the addition of (R)-2-chloromethyl-oxirane (1.85 g, 20 mmol). The reaction solution was stirred for 5 hours and concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography to obtain the title compound tert-butyl 4-[[(2R)-oxiran-2-yl]methyl]piperazine-1-carboxylate 7b (3.55 g, yield: 74.0%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691822B2
Source datasetuspto-grants-2014_04
ORD IDord-7ef6743e6cd14c99a129e5c779268a2d
Source noteuspto-grants-2014_04