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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1655171Generated: November 2, 2026

3-Chloro-2-hydrazinyl-5-(trifluoromethyl)pyridine → HCID 1475765, compound

https://huagongshe.com/reaction/1655171

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chloro-2-hydrazinyl-5-(trifluoromethyl)pyridineHCID 1272691—
ReactantEthyl 2-acetyl-3-(dimethylamino)acrylateHCID 3806790—
SolventEthanolHCID 702—
ProductHCID 1475765HCID 147576569.8%

Reaction Steps

A stirred solution of 44.0 grams (0.21 mole) of 3-chloro-5-trifluoromethylpyridin-2-ylhydrazine and 38.6 grams (0.21 mole) of ethyl 2-acetyl-3-dimethylaminoacrylate, prepared by the method of J. R. Beck et al., J. Het. Chem., 24, 693 (1987), in 1000 mL of ethanol was heated at reflux for five hours. After this time, the reaction mixture was cooled to ambient temperature and concentrated under reduced pressure to a residual oil. The oil was taken up in methylene chloride and washed in succession with two 100 mL portions of aqueous 10% hydrochloric acid, an aqueous solution saturated with sodium bicarbonate, and water. The organic layer was dried and filtered. The filtrate was concentrated under reduced pressure, yielding 48.9 grams of 4-ethoxycarbonyl-5-methyl-1-(3-chloro-5-trifluoromethylpyridin-2-yl)-1H-pyrazole. The nmr spectrum was consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05250504
Source datasetuspto-grants-1993_10
ORD IDord-6e417c1c4bc7423395719399d615f3bb
Source noteuspto-grants-1993_10