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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1241452Generated: October 31, 2026

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

https://huagongshe.com/reaction/1241452

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 the sodium salt of ethyl cyanopyruvate (preparation in analogy to Borsche and Manteuffel, Liebigs Ann. 1934, 512, 97) in 2.51 of dioxane under argon with efficient stirring at room temperature, and the mixture is stirred for 10 min, during which most of the precursor dissolves. Then 85.93 g (0.613 mol) of 2-fluorobenzyl-hydrazine are added, and the mixture is boiled overnight. After cooling, the sodium trifluoroacetate crystals which have separated out are filtered off with suction and washed with dioxane, and the crude solution is reacted further.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07115599B2
Source datasetuspto-grants-2006_10
ORD IDord-c6ccc52bc05a4100ab0d1265052dab4b
Source noteuspto-grants-2006_10