HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 406597Generated: October 26, 2026
Methylhydrazine → ethyl 5-(2,6-difluorophenyl)-1-methyl-1H-pyrazole-3-carboxylate
https://huagongshe.com/reaction/406597
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methylhydrazine | HCID 6061 | — |
| Reactant | Diethyl Oxalate | HCID 7268 | — |
| Reactant | 1-(2,6-Difluorophenyl)ethan-1-one | HCID 83643 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | ethyl 5-(2,6-difluorophenyl)-1-methyl-1H-pyrazole-3-carboxylate | HCID 66613940 | 12.5% |
Reaction Steps
To a mixture of 2,6-difluoroacetophenone (4.7 g, 0.03 mol) and 1,2-diethyl ethanedioate (4.8 g, 0.033 mol) in ethanol (33 mL) was added sodium tert-butoxide (3.17 g, 0.033 mol). After 1 h, more ethanol (30 mL) was added to the reaction mixture and stirring was continued for 1 h. The reaction mixture was partitioned between hydrochloric acid (1 N) and diethyl ether. The organic phase was separated, dried over magnesium sulfate, filtered, and concentrated under reduced pressure to half its original volume. To the resulting mixture was added methylhydrazine (1.52 g, 0.033 mol) and stirring was continued overnight. The reaction mixture was concentrated under reduced pressure and the resulting material was purified by silica gel chromatography (5 to 20% gradient of ethyl acetate in methylene chloride as eluant) to provide the title compound as a solid (1.0 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08754115B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-346fa9d45dff41edac41bda2c0541f34 |
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| Source note | uspto-grants-2014_06 |
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