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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1440748Generated: October 26, 2026

Triethylamine → Ethyl 1,4-dibenzylpiperazine-2-carboxylate

https://huagongshe.com/reaction/1440748

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBenzathineHCID 8793—
ReactantEthyl 2,3-dibromopropionateHCID 97945—
ReactantTriethylammonium bromideHCID 2734074—
SolventBenzeneHCID 241—
ProductEthyl 1,4-dibenzylpiperazine-2-carboxylateHCID 273640289%

Reaction Steps

80 g (0.31 mol) of ethyl 2,3-dibromopropionate diluted in 300 ml of benzene are added dropwise, but fairly rapidly, to a warm solution of 72 g (0.3 mol) of N,N'-dibenzylethylenediamine, 700 ml of benzene and 50 ml (0.36 mol) of triethylamine. After the addition, reflux is maintained for 3 hours (triethylamine hydrobromide precipitates in the reaction mixture). The mixture is cooled and filtered through fritted glass, and the solid is washed with ether. The filtrate is washed with 200 ml of saturated sodium hydrogen carbonate solution and then twice with 100 ml of water. The organic phases are dried over magnesium sulfate and the solvents are evaporated off in vacuo. Approximately 100 ml of toluene are added, and evaporation is continued. The resulting residue is diluted in 400 ml of absolute ethanol and saturated with gaseous hydrogen chloride. The salt precipitates by the addition of ether. Filtering, washing with ether and drying yield from 100 to 110 g of white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05500426
Source datasetuspto-grants-1996_03
ORD IDord-4e8c728510c3408ea248a1e279aa0355
Source noteuspto-grants-1996_03