HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2164906Generated: October 25, 2026
1,2-Dimethylhydrazine → 3-(2-Aminoethylamino)-1,2,4-trimethylpyrazol-5-one
https://huagongshe.com/reaction/2164906
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dimethylhydrazine | HCID 1322 | — |
| Reactant | Diethyl methylmalonate | HCID 11857 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 3-Hydroxy-1,2,4-trimethyl-5-pyrazolone | HCID 12818853 | — |
| Reactant | 3-Chloro-1,2,4-trimethylpyrazol-5-one | HCID 12818854 | — |
| Product | 3-(2-Aminoethylamino)-1,2,4-trimethylpyrazol-5-one | HCID 12818855 | — |
Reaction Steps
The 3-chloro-1,2,4-trimethylpyrazol-5-one used as starting material can be obtained in the following manner: 28.6 g. 3-hydroxy-1,2,4-trimethylpyrazol-5-one (m.p. 87°-89° C., after recrystallization from ethyl acetate), prepared from diethyl methylmalonate and N,N'-dimethylhydrazine, are boiled under reflux for 3.5 hours with 55 ml. phosphorus oxychloride. The reaction mixture is then evaporated and the residue is stirred with ice and water, rendered alkaline by the addition of 10N aqueous sodium hydroxide solution and extracted 8 times with 100 ml. amounts of methylene chloride. The combined extracts are then dried and evaporated to give 24.7 g. (76.5% of theory) 3-chloro-1,2,4-trimethylpyrazol-5-one in the form of colorless crystals; m.p. 37°-38° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04507488 |
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| Source dataset | uspto-grants-1985_03 |
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| ORD ID | ord-fb3ef9226dad4925a7e1936de36c70f8 |
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| Source note | uspto-grants-1985_03 |
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