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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2250325Generated: October 31, 2026

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

https://huagongshe.com/reaction/2250325

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 (prepared in analogy to Borsche and Manteuffel, Liebigs Ann. 1934, 512, 97) while stirring efficiently in 2.5 l of dioxane at room temperature under argon, and the mixture is stirred for 10 min, during which most of the precursor dissolves. Then 85.93 g (0.613 mol) of 2-fluorobenzylhydrazine 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 numberUS07317016B2
Source datasetuspto-grants-2008_01
ORD IDord-63b79969112746a494732fa7f12ecd2a
Source noteuspto-grants-2008_01