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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2163523Generated: November 3, 2026

5-Chloro-1,3-dimethyl-n-phenyl-1h-pyrazole-4-carboxamide → 1,3-Dimethyl-N-phenyl-1H-pyrazole-4-carboxamide

https://huagongshe.com/reaction/2163523

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Chloro-1,3-dimethyl-n-phenyl-1h-pyrazole-4-carboxamideHCID 73028—
ReactantSodium AcetateHCID 517045—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product1,3-Dimethyl-N-phenyl-1H-pyrazole-4-carboxamideHCID 1303172796%

Reaction Steps

5-chloro-1,3-dimethyl-N-phenyl-4-pyrazolecarboxamide (2.7 g) was dissolved in ethanol (100 ml) and anhydrous sodium acetate (2 g) added. The mixture was hydrogenated at room temperature and 2 atmospheres pressure using palladium on carbon catalyst. On completion of the reaction, the catalyst was removed by filtration through celite and the filtrate evaporated in vacuo. Water (50 ml) was added and the product extracted with chloroform (3 × 25 ml). The combined extracts were washed with water, dried and evaporated. The product was crystallised from ethanol and 1,3-dimethyl-N-phenyl-4-pyrazolecarboxamide (2 g, 96%) was obtained as colourless needles, m.p. 91-92° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04134987
Source datasetuspto-grants-1979_01
ORD IDord-a4c1f2f677254cfbadd2c1b512be0564
Source noteuspto-grants-1979_01