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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 8074Generated: October 28, 2026

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

https://huagongshe.com/reaction/8074

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 numberUS07087634B2
Source datasetuspto-grants-2006_08
ORD IDord-96385c6264c1424398d9348e12f7a5f7
Source noteuspto-grants-2006_08