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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 379606Generated: October 26, 2026

Carbon Dioxide → (2S,5R)-1-allyl-2,5-dimethylpiperazine

https://huagongshe.com/reaction/379606

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantTolueneHCID 1140—
ReactantPotassium HydroxideHCID 14797—
ReactantEthyl trans-4-allyl-2,5-dimethyl-1-piperazinecarboxylateHCID 10823138—
SolventEthanolHCID 702—
Product(2S,5R)-1-allyl-2,5-dimethylpiperazineHCID 1129119169%

Reaction Conditions

Temperature100 °C

Reaction Steps

Ethyl trans-4-allyl-2,5-dimethyl-1-piperazinecarboxylate (630 g, 2.78 mol) was added to a solution of 87% potassium hydroxide pellets (2970 g, 46 mol) in 4300 mL of 95% ethanol and heated at reflux for 1.5 hours. Carbon dioxide evolution was observed for the first 0.5-1 hour of heating. The reaction was cooled below reflux temperature and 2000 mL of toluene was carefully added. Ethanol was removed by azeotropic distillation at 105° C., while adding an additional 4000 mL of toluene to the reaction flask during the course of the distillation. After collection of 9000 mL of distillate, the reaction was cooled to 100° C. and 1000 mL of toluene was carefully added. The solution was slowly cooled to 5° C. and maintained at 5° C. for 30 minutes. The solution was filtered, washing the filter cake with an additional 1500 mL of toluene. The filtrate was washed with 1000 mL of water, dried over magnesium sulfate, and the solvent was removed to give 296 g (69%) of trans-1-allyl-2,5-dimethylpiperazine as a dark liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06300332B1
Source datasetuspto-grants-2001_10
ORD IDord-5b8fdfd094a146f69efa8d2437709435
Source noteuspto-grants-2001_10