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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 67164Generated: October 29, 2026

Potassium Hydroxide → N-[5-oxo-1-(2,4,6-trichlorophenyl)-2-pyrazolin-3-yl]acetamide

https://huagongshe.com/reaction/67164

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactant4,5-dihydro-1H-pyrazol-5-oneHCID 316289—
Reactant1,2,4-OxadiazoleHCID 6451463—
Reactant2-(5-Methyl-1,2,4-oxadiazol-3-yl)-N-(2,4,6-trichlorophenyl)acetamideHCID 13380563—
SolventEthanolHCID 702—
ProductN-[5-oxo-1-(2,4,6-trichlorophenyl)-2-pyrazolin-3-yl]acetamideHCID 4497701—

Reaction Conditions

Temperature80 °C

Reaction Steps

The method of the invention is then used to convert the 1,2,4-oxadiazole to the 2-pyrazolin-5-one. As previously described, the method comprises forming a liquid reaction system of a base catalyst and the 1,2,4-oxadiazole in an organic liquid reaction medium and heating the reaction system to a temperature sufficient to cause the 1,2,4-oxadiazole to be rearranged to the 2-pyrazolin-5-one, e.g., heating a solution of potassium hydroxide and 2-(5-methyl-1,2,4-oxadiazol-3-yl)-2',4',6'-trichloroacetanilide in anhydrous ethanol under reflux at a temperature of 80° C. for 8 to 14 hours to yield 3-acetamido-1-(2,4,6-trichlorophenyl)-2-pyrazolin-5-one, i.e., ##STR7##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04345085
Source datasetuspto-grants-1982_08
ORD IDord-fb048cce53cd4d838277eec7545f618d
Source noteuspto-grants-1982_08