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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 1-Ethyl-4-(prop-2-ynyl)piperazine | HCID 21190741 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 4-(N-ethylpiperazino)-2-butynoic acid | HCID 11805649 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06251912B1 |
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| Source dataset | uspto-grants-2001_06 |
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| ORD ID | ord-8e9c9e47f10741cd9e265c02c38fc5fa |
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| Source note | uspto-grants-2001_06 |
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