HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1360441Generated: October 31, 2026
Ethyl 2,4-dioxovalerate → Ethyl 1-ethyl-5-methyl-1H-pyrazole-3-carboxylate
https://huagongshe.com/reaction/1360441
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl 2,4-dioxovalerate | HCID 69208 | — |
| Reactant | Hydrazine, ethyl-, ethanedioate (1:1) | HCID 96181 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 1-ethyl-5-methyl-1H-pyrazole-3-carboxylate | HCID 16394811 | 100.5% |
Reaction Steps
Ethylhydrazine oxalate (23.7 g, 158 mmol) was added slowly to an 11° C. solution of ethyl acetopyruvate (50.0 g, 316 mmol) in ethanol so that the internal temperature did not exceed 14° C. The reaction was allowed to warm to ambient temperature and was stirred overnight. The reaction was concentrated under reduced pressure and 2 M sodium carbonate was added to adjust the mixture to pH 9. The mixture was transferred to a separatory funnel. The aqueous phase was extracted with methyl tert-butyl ether (3×600 mL). The organic layers were combined, dried over magnesium sulfate, filtered, and concentrated under reduced pressure to yield 28.94 g of ethyl 1-ethyl-5-methyl-1H-pyrazole-3-carboxylate as an orange oil that was used without purification in the next reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07879849B2 |
|---|
| Source dataset | uspto-grants-2011_02 |
|---|
| ORD ID | ord-08d9deb8acff49c891f04e4b57649dd2 |
|---|
| Source note | uspto-grants-2011_02 |
|---|