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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 413773Generated: October 29, 2026

Ammonium formate → Ethyl 1-(4-aminophenyl)-5-(trifluoromethyl)-1H-pyrazole-4-carboxylate

https://huagongshe.com/reaction/413773

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
ReactantEthyl 1-(4-nitrophenyl)-5-(trifluoromethyl)-1H-pyrazole-4-carboxylateHCID 2737215—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductEthyl 1-(4-aminophenyl)-5-(trifluoromethyl)-1H-pyrazole-4-carboxylateHCID 2808376—

Reaction Steps

To 1-(4-nitrophenyl)-5-trifluoromethyl-1H-pyrazole-4-carboxylic acid ethyl ester (0.5 g, 1.5 mmol) dissolved in methanol (4 mL) was added palladium on carbon and ammonium formate (0.428 g, 6.8 mmol). This mixture was stirred at room temperature overnight. The solvent was removed under vacuum, then the material was resuspended in chloroform, and washed with water (twice) and saturated sodium bicarbonate (once), and the organic layer dried over magnesium sulfate (MgSO4). The solid was filtered and the solvents removed under vacuum. The reaction product was purified over silica gel to yield the named product (m.p. 102° C.-103° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06569885B1
Source datasetuspto-grants-2003_05
ORD IDord-790b99883c7f41afa410293494686840
Source noteuspto-grants-2003_05