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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 4,4,4-trifluoroacetoacetateHCID 67793—
Reactant5-Chloro-2-hydrazinylpyridineHCID 13590464—
SolventAcetic AcidHCID 176—
ProductHCID 178516155HCID 17851615553.9%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05750550
Source datasetuspto-grants-1998_05
ORD IDord-c4cd6134d6d241f181a3ef0c2155d47b
Source noteuspto-grants-1998_05