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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1266251Generated: October 25, 2026

Carbon Dioxide → 4-[(2-Methoxy-ethyl)-methyl-amino]-but-2-ynoic acid

https://huagongshe.com/reaction/1266251

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantWaterHCID 962—
Reactant(2-Methoxyethyl)(methyl)(prop-2-yn-1-yl)amineHCID 18548974—
ReactantButyllithiumHCID 178418339—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product4-[(2-Methoxy-ethyl)-methyl-amino]-but-2-ynoic acidHCID 18548968—

Reaction Conditions

Temperature-78 °C

Reaction Steps

n-Butyl lithium in hexane (37.8 mL, 2.5 M in n-hexane) was slowly added to (2-methoxy-ethyl)-methyl-prop-2-ynyl-amine (12.0 g, 94.5 mmol) in 90 mL of tetrahydrofuran under nitrogen. The mixture was stirred for 1 hr at −78° C., then dry carbon dioxide was passed through the reaction 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 15 g of 4-[(2-methoxy-ethyl)-methyl-amino]-but-2-ynoic acid: mass spectrum (m/e): M−H 170.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06548496B2
Source datasetuspto-grants-2003_04
ORD IDord-06e88d9b5be54de38434fff4de872cc4
Source noteuspto-grants-2003_04