HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 30620Generated: October 29, 2026
Ethyl Acetoacetate → HCID 69205750, compound
https://huagongshe.com/reaction/30620
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetoacetate | HCID 8868 | — |
| Reactant | 4-Fluorobenzoic acid N-methylhydrazide | HCID 45075708 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 69205750 | HCID 69205750 | 44% |
Reaction Steps
A mixture of 4-fluoro-N-methylbenzohydrazide (5.0 g), ethyl acetoacetate (4.84 g) and ethanol (140 ml) was stirred for 14 hrs. with heating under reflux. The reaction mixture was concentrated, water was added, and the mixture was extracted with ethyl acetate. The organic layer was washed with water, dried over anhydrous magnesium sulfate and concentrated. The residue was subjected to silica gel column chromatography to give an oil from a fraction eluted with hexane-ethyl acetate (4:1-1:1, v/v). This oil was dissolved in ethanol (50 ml), 1,8-diazabicyclo[5.4.0]-7-undecene (0.5 ml) was added, and the mixture was stirred for 4 hrs. with heating under reflux. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with water, dried over anhydrous magnesium sulfate and concentrated to give ethyl 5-(4-fluorophenyl)-1,3-dimethyl-1H-pyrazole-4-carboxylate (3.41 g, yield 44%) as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07423159B2 |
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| Source dataset | uspto-grants-2008_09 |
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| ORD ID | ord-5dd5c739e64f4e12a9259ec84e2ff7af |
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| Source note | uspto-grants-2008_09 |
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