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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 8570Generated: October 28, 2026

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

https://huagongshe.com/reaction/8570

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 100.00 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-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 remaining crude solution is reacted further.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07091198B1
Source datasetuspto-grants-2006_08
ORD IDord-347c075934a74b70a106dd279acbdf62
Source noteuspto-grants-2006_08