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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2393308Generated: October 31, 2026

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

https://huagongshe.com/reaction/2393308

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 numberUS05807858
Source datasetuspto-grants-1998_09
ORD IDord-437111fe838c4b78a6ee4056c0b5a77e
Source noteuspto-grants-1998_09