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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1068980Generated: October 26, 2026

Carbon Dioxide → 4-(N-ethylpiperazino)-2-butynoic acid

https://huagongshe.com/reaction/1068980

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantWaterHCID 962—
Reactant1-Ethyl-4-(prop-2-ynyl)piperazineHCID 21190741—
ReactantButyllithiumHCID 178418339—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product4-(N-ethylpiperazino)-2-butynoic acidHCID 11805649—

Reaction Conditions

Temperature-78 °C

Reaction Steps

n-Butyl lithium in hexane (42 mL, 2.5M in n-hexane) was slowly added to 1-ethyl-4-prop-2-ynyl-piperazine (16 g, 105 mmol) in 80 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 18 g of 4-(4-ethyl-piperazin-1-yl)-but-2-ynoic acid: mass spectrum (m/e):M−H 195.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06251912B1
Source datasetuspto-grants-2001_06
ORD IDord-8e9c9e47f10741cd9e265c02c38fc5fa
Source noteuspto-grants-2001_06