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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1900263Generated: October 29, 2026

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

https://huagongshe.com/reaction/1900263

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) in2500 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 1M 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 numberUS05574159
Source datasetuspto-grants-1996_11
ORD IDord-a2628f275c5f43029d4f7b9f27a695e1
Source noteuspto-grants-1996_11