Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 548455Generated: October 29, 2026

Carbon Dioxide → 4-(4-Methylpiperazin-1-yl)but-2-ynoic acid

https://huagongshe.com/reaction/548455

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantWaterHCID 962—
Reactant1-Methyl-4-(prop-2-yn-1-yl)piperazineHCID 13514091—
ReactantButyllithiumHCID 178418339—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product4-(4-Methylpiperazin-1-yl)but-2-ynoic acidHCID 18548981—

Reaction Conditions

Temperature-78 °C

Reaction Steps

n-Butyl lithium in hexane (17.2 mL, 2.5M in n-hexane) was slowly added to 1-methyl-4-prop-2-ynyl-piperazine (6.0 g, 43.5 mmol) in 40 mL of tetrahydrofuran under nitrogen. The mixture was stirred for 1 hr at −78° C., then dry carbon dioxide was passed through overnight. The resulting solution was poured into water and washed with ethyl acetate. The aqueous layer was evaporated under reduced pressure to give the crude acid. The dry acid was dissolved in methanol, and the insoluble salt was removed via filtration. The filtrate was collected and dried in vacuo to give 7 g of 4-(4-methyl-piperazin-1-yl)-but-2-ynoic acid: mass spectrum (m/e): M−H 181.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE042376E1
Source datasetuspto-grants-2011_05
ORD IDord-a0f31fd0f14d4f62a20fdf7b28db26cd
Source noteuspto-grants-2011_05