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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 346526Generated: October 30, 2026

Trifluoroacetic acid → ethyl 5-amino-1-(2-fluorobenzyl)-1H-pyrazole-3-carboxylate

https://huagongshe.com/reaction/346526

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodiumHCID 5360545—
Reactant(2-Fluorobenzyl)hydrazineHCID 10374537—
ReactantEthyl 3-cyano-2-oxopropanoateHCID 11309560—
Solvent1,4-DioxaneHCID 31275—
Productethyl 5-amino-1-(2-fluorobenzyl)-1H-pyrazole-3-carboxylateHCID 11391384—

Reaction Steps

111.75 g (75 ml, 0.98 mol) of trifluoroacetic acid are added to 100 g (0.613 mol) of sodium salt of ethyl cyanopyruvate (prepared in analogy to Borsche and Manteuffel, Liebigs Ann. 1934, 512, 97) in 2.5 l of dioxane under argon with efficient stirring at room temperature, and the mixture is stirred for 10 minutes during which much of the precursor dissolves. Then 85.93 g (0.613 mol) of 2-fluorobenzylhydrazine are added, and the mixture is heated under reflux overnight. After cooling, the crystals of sodium trifluoroacetate which have separated out are filtered off with suction and washed with dioxane, and the solution is reacted further as it is.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07173037B2
Source datasetuspto-grants-2007_02
ORD IDord-9a5b697519de4de7926276d57e7d7215
Source noteuspto-grants-2007_02