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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1038612Generated: November 2, 2026

Allyl bromide → Ethyl trans-4-allyl-2,5-dimethyl-1-piperazinecarboxylate

https://huagongshe.com/reaction/1038612

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantSodium CarbonateHCID 10340—
ReactantEthyl trans-2,5-dimethyl-1-piperazinecarboxylateHCID 10607598—
SolventAcetonitrileHCID 6342—
ProductEthyl trans-4-allyl-2,5-dimethyl-1-piperazinecarboxylateHCID 1082313881%

Reaction Steps

A mixture of ethyl trans-2,5-dimethyl-1-piperazinecarboxylate (643 g, 3.45 mol), allyl bromide (328 mL, 3.80 mol), and sodium carbonate (440 g, 4.15 mol) in 2500 mL of acetonitrile was heated at reflux for 1.5 hours. The reaction was cooled to room temperature, filtered, and the solvent removed under vacuum. The residue was dissolved in 4000 mL of dichloromethane and washed with two 500 mL portions of 1 M sodium hydroxide. The dichloromethane solution was dried over magnesium sulfate and the solvent was removed to give 630 g (81%) of ethyl trans-4-allyl-2,5-dimethyl-1-piperazinecarboxylate as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08551998B2
Source datasetuspto-grants-2013_10
ORD IDord-536017d75da94dd0bd36afdd4dec52d7
Source noteuspto-grants-2013_10