HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1289856Generated: October 26, 2026
Ethyl 4,4,4-trifluoroacetoacetate → HCID 178516155, compound
https://huagongshe.com/reaction/1289856
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl 4,4,4-trifluoroacetoacetate | HCID 67793 | — |
| Reactant | 5-Chloro-2-hydrazinylpyridine | HCID 13590464 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 178516155 | HCID 178516155 | 53.9% |
Reaction Steps
A mixture of 1.445 g (10 mmol) of 2-hydrazino-5-chloropyridine and ethyl trifluoroacetoacetate (1.5 ml; 10 mmol) in 5 ml of acetic acid was refluxed overnight with stirring under nitrogen and then cooled. The mixture was concentrated in vacuo, the residue was diluted with ethyl acetate, and the solid mixture was filtered. The filtrate was washed with saturated sodium bicarbonate solution, the aqueous layer was extracted with ethyl acetate, and the combined organic layer was dried over magnesium sulfate. The organic layer was concentrated in vacuo, the residue was purified by flash chromatography (ethyl acetate) and crystallized (from ethyl acetate/hexane followed by hexane) to afford 1.42 g of 1-(5-chloro-2-pyridyl)-3-trifluoromethyl-5-hydroxy-pyrazole as a white solid, m.p. 58°-59° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05750550 |
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| Source dataset | uspto-grants-1998_05 |
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| ORD ID | ord-c4cd6134d6d241f181a3ef0c2155d47b |
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| Source note | uspto-grants-1998_05 |
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