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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DimethylhydrazineHCID 1322—
ReactantDiethyl methylmalonateHCID 11857—
ReactantPhosphorus oxychlorideHCID 24813—
Reactant3-Hydroxy-1,2,4-trimethyl-5-pyrazoloneHCID 12818853—
Reactant3-Chloro-1,2,4-trimethylpyrazol-5-oneHCID 12818854—
Product3-(2-Aminoethylamino)-1,2,4-trimethylpyrazol-5-oneHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04507488
Source datasetuspto-grants-1985_03
ORD IDord-fb3ef9226dad4925a7e1936de36c70f8
Source noteuspto-grants-1985_03