HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1708854Generated: November 3, 2026
Pyrazole → 1-(2,4,6-Trichlorophenyl)-3-acetylamino-4-pyrazolyl-5-oxo-2pyrazoline
https://huagongshe.com/reaction/1708854
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyrazole | HCID 1048 | — |
| Reactant | 1-(2,4,6-Trichlorophenyl)-3-acetylamino-4-bromo-5-oxo-2-pyrazoline | HCID 12994776 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-(2,4,6-Trichlorophenyl)-3-acetylamino-4-pyrazolyl-5-oxo-2pyrazoline | HCID 178474494 | 34.7% |
Reaction Steps
Next, 57 g (0.15 mol) of the 1-(2,4,6-trichlorophenyl)-3-acetylamino-4-bromo-5-oxo-2-pyrazoline and 41 g of pyrazole (0.6 mol) were mixed well, then heated for 6 hours at 75° C. in a stream of nitrogen gas to react, after which the reaction mixture was cooled to room temperature. Next the reaction mixture was dissolved in ethyl acetate and the solution was washed with water three times and then dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, acetonitrile was added to the residual oil, and the deposited crystals were filtered to obtain 20.1 g (34.7%) of 1-(2,4,6-trichlorophenyl)-3-acetylamino-4-pyrazolyl-5-oxo-2pyrazoline.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04946771 |
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| Source dataset | uspto-grants-1990_08 |
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| ORD ID | ord-46a980f9805a405f9046d2dc1a11c967 |
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| Source note | uspto-grants-1990_08 |
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