HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenylhydrazine → Ethyl 3-methyl-1-phenylpyrazole-5-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenylhydrazine | HCID 7516 | — |
| Reactant | Ethyl 2,4-dioxovalerate | HCID 69208 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | Ethyl 3-methyl-1-phenylpyrazole-5-carboxylate | HCID 2746772 | — |
| Product | Ethyl 5-methyl-1-phenyl-1H-pyrazole-3-carboxylate | HCID 10900438 | — |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
2 ml ethyl 2,4-dioxovalerate and 1.2 g phenyl hydrazine were dissolved in 20 ml acetic acid, followed by stirring at 100° C. for 2 hours. After evaporating acetic acid, ethyl acetate was added to the residue. The mixture was washed with aqueous sodium hydrogencarbonate solution and brine, dried over anhydrous magnesium sulfate and evaporated. The residue was subjected to silica gel column chromatography, to give 0.37 g of ethyl 3-methyl-1-phenyl-1H-5-pyrazolecarboxylate with hexane:ethyl acetate (14:1) and 0.46 g of ethyl 5-methyl-1-phenyl-1H-3-pyrazolecarboxylate with hexane:ethyl acetate (9:1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06884821B1 |
| Source dataset | uspto-grants-2005_04 |
| ORD ID | ord-f288b1ed3a0a4d9b8821f343cbfd88bf |
| Source note | uspto-grants-2005_04 |