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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 402739Generated: October 29, 2026

Ethyl 2-ethoxy-4-oxo-4,5-dihydrofuran-3-carboxylate → Ethyl 4-oxo-2-{[4-(2,2,2-trifluoroethyl)piperazinyl]amino}-4,5-dihydrofuran-3-carboxylate

https://huagongshe.com/reaction/402739

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-ethoxy-4-oxo-4,5-dihydrofuran-3-carboxylateHCID 13791062—
Reactant4-(2,2,2-Trifluoroethyl)piperazin-1-amineHCID 80035743—
SolventEthanolHCID 702—
ProductEthyl 4-oxo-2-{[4-(2,2,2-trifluoroethyl)piperazinyl]amino}-4,5-dihydrofuran-3-carboxylateHCID 86708414—

Reaction Steps

To a solution of 4-(2,2,2-trifluoroethyl)piperazine-1-amine (4.72 g, 25.8 mmol) in ethanol (43 mL), ethyl 2-ethoxy-4-oxo-4,5-dihydrofuran-3-carboxylate (4.70 g, 23.5 mmol) which similarly prepared according to the procedure described in the Example 74, Third step was added at ambient temperature. The mixture was stirred for 2 h. The precipitate was collected by filtration, washed with diethyl ether and hexane then dried to afford ethyl 4-oxo-2-{[4-(2,2,2-trifluoroethyl)piperazinyl]amino}-4,5-dihydrofuran-3-carboxylate as solid (5.64 g, y. 71%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08742113B2
Source datasetuspto-grants-2014_06
ORD IDord-4d39176845a5446dbc3da72c37974a13
Source noteuspto-grants-2014_06