Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 379152Generated: October 30, 2026

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

https://huagongshe.com/reaction/379152

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 numberUS06297258B1
Source datasetuspto-grants-2001_10
ORD IDord-8ca7729d44f441c39846108927807ef7
Source noteuspto-grants-2001_10