HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2395219Generated: November 4, 2026
Acetylacetone → Pyrazole-1-carboxamidine, 3,5-dimethyl-, monohydrochloride
https://huagongshe.com/reaction/2395219
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetylacetone | HCID 31261 | — |
| Reactant | HCID 178418668 | HCID 178418668 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Pyrazole-1-carboxamidine, 3,5-dimethyl-, monohydrochloride | HCID 218002 | — |
Reaction Steps
To 850 ml of ethanol were added 188 g of aminoguanidine hydrochloride and 170 g of 2,4-pentadione and the mixture was heated with stirring for 3 hrs. under reflux. The precipitated crystals were filtered, sufficiently washed with ethanol and dried to obtain 1-amidino-3,5-dimethylpyrazole hydrochloride of 210 g. Next, 60 g of potassium hydroxide was dissolved in water of 120 g and 1-amidino-3,5-dimethylpyrazole hydrochloride of 61.1 g was added thereto withcooling with water and stirred further for 1 hr. Chloroform of 200 ml was added to the solution for extraction. A chloroform layer was separated, washed with water and dried with anhydrous sodium sulfate, thereafter, chloroform was removed to obtain 1-amidino-3,5-dimethylpyrazole of 46.0 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05814580 |
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| Source dataset | uspto-grants-1998_09 |
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| ORD ID | ord-6e4a46c9168b4937af9c4670035661f1 |
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| Source note | uspto-grants-1998_09 |
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