HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Chloro-1,3-dimethyl-n-phenyl-1h-pyrazole-4-carboxamide → 1,3-Dimethyl-N-phenyl-1H-pyrazole-4-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Chloro-1,3-dimethyl-n-phenyl-1h-pyrazole-4-carboxamide | HCID 73028 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1,3-Dimethyl-N-phenyl-1H-pyrazole-4-carboxamide | HCID 13031727 | 96% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04134987 |
| Source dataset | uspto-grants-1979_01 |
| ORD ID | ord-a4c1f2f677254cfbadd2c1b512be0564 |
| Source note | uspto-grants-1979_01 |