HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 977006Generated: October 25, 2026
Methylhydrazine → Ethyl 5-ethyl-1-methyl-1H-pyrazole-3-carboxylate
https://huagongshe.com/reaction/977006
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methylhydrazine | HCID 6061 | — |
| Reactant | Ethyl-2,4-dioxohexanoate | HCID 61590 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | Ethyl 5-ethyl-1-methyl-1H-pyrazole-3-carboxylate | HCID 22145397 | — |
Reaction Steps
Ethyl 2,4-dioxohexanoate (12 g) in glacial acetic acid (75 ml) was cooled in an ice-bath and treated with methylhydrazine (3.21 g) in a dropwise fashion over 5-10 m. On complete addition the ice cooling was removed and the yellow homogeneous solution stirred at room temperature for ca. 2 h. The acetic acid was then removed in vacuo and the residual oil re-dissolved in ethyl acetate (~ 100 mls). The ethyl acetate solution was washed with saturated sodium hydrogen carbonate (3×) and brine. After drying over anhydrous magnesium sulphate the solvent was evaporated. The crude material was purified by silica gel chromatography eluting with 20-70% ethyl acetate/hexane giving the title compound as a pale yellow oil, (6.656 g, 52%); dH (CDCl3) 1.28 (3H, t, J7.6 Hz), 1.38 (3H, t, J7.1 Hz), 2.61 (2H, q, J7.6 Hz), 3.84 (3H, s), 4.38 (2H, q, J7.1 Hz) and 6.58 (1H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05612477 |
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| Source dataset | uspto-grants-1997_03 |
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| ORD ID | ord-184c2c38406b4848ac412c165e6b07a8 |
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| Source note | uspto-grants-1997_03 |
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