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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 4,5-dihydro-1H-pyrazol-5-one | HCID 316289 | — |
| Reactant | 1,2,4-Oxadiazole | HCID 6451463 | — |
| Reactant | 2-(5-Methyl-1,2,4-oxadiazol-3-yl)-N-(2,4,6-trichlorophenyl)acetamide | HCID 13380563 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-[5-oxo-1-(2,4,6-trichlorophenyl)-2-pyrazolin-3-yl]acetamide | HCID 4497701 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04345085 |
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| Source dataset | uspto-grants-1982_08 |
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| ORD ID | ord-fb048cce53cd4d838277eec7545f618d |
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| Source note | uspto-grants-1982_08 |
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