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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2243270Generated: October 26, 2026

p-Toluenesulfonic acid → 1-(3-methyl-4-nitrobenzyl)-5-pentafluoroethyl-1H-pyrazole

https://huagongshe.com/reaction/2243270

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant5-Ethoxy-1,1,1,2,2-pentafluoro-4-penten-3-oneHCID 3729085—
Reactant[(3-Methyl-4-nitrophenyl)methyl]hydrazineHCID 20367228—
SolventEthanolHCID 702—
Product1-(3-methyl-4-nitrobenzyl)-5-pentafluoroethyl-1H-pyrazoleHCID 86076299—
Product1-(3-methyl-4-nitrobenzyl)-3-pentafluoroethyl-1H-pyrazoleHCID 86076301—

Reaction Steps

(3-Methyl-4-nitrobenzyl)-hydrazine (1.81 g) and 5-ethoxy-1,1,1,2,2-pentafluoro-4-penten-3-one (2.18 g) were refluxed in ethanol (60 ml) for 8 hours, and p-toluenesulfonic acid (0.10 g) was added thereto and the mixture was further refluxed for 6 hours. After finishing the reaction, the solvent was distilled off and the obtained residue was purified by silica gel column chromatography (mixed solvent of n-hexane and ethyl acetate) to obtain 1-(3-methyl-4-nitrobenzyl)-5-pentafluoroethyl-1H-pyrazole (0.96 g) as the first elution portion and 1-(3-methyl-4-nitrobenzyl)-3-pentafluoroethyl-1H-pyrazole (0.50 g) as the second elution portion.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07674807B2
Source datasetuspto-grants-2010_03
ORD IDord-b0e3e501ad744800bac8c0722182f726
Source noteuspto-grants-2010_03