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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 462416Generated: October 30, 2026

Ethyl 3-(thiophen-2-yl)piperazine-1-carboxylate → 1-Methyl-3-(thiophen-2-yl)piperazine

https://huagongshe.com/reaction/462416

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 3-(thiophen-2-yl)piperazine-1-carboxylateHCID 2771741—
ReactantAluminium lithium hydrideHCID 21226445—
SolventDiethyl EtherHCID 3283—
Product1-Methyl-3-(thiophen-2-yl)piperazineHCID 13048186—

Reaction Steps

A solution of ethyl 3-(2-thienyl)piperazine-carboxylate (27.2 g, 0.11 mol; Preparation 2) in diethyl ether (300 ml) is added to a stirred suspension of lithium aluminum hydride (10.8 g, 0.28 mol) in diethyl ether (1300 ml). The mixture is refluxed for 12 h, cooled to room temperature and worked up as described in "Reagents for Organic Synthesis" , Fieser, L. F. and Fieser, M., John Wiley and Sons, Inc., New York, N.Y. 1967, p. 583. The ether solution is dried (potassium carbonate) and evaporated to give 1-methyl-3-(2-thienyl)piperazine as a light yellow oil, which is characterized as the maleate salt (m.p. 123°-124.5° C.), which is prepared in the manner described in Preparation 2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04515792
Source datasetuspto-grants-1985_05
ORD IDord-0463835542f8453ea4640b1ef8cf8d9f
Source noteuspto-grants-1985_05