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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1952746Generated: October 26, 2026

Phenylhydrazine → 1-Phenyl-1H-pyrazole-3,5-diamine

https://huagongshe.com/reaction/1952746

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylhydrazineHCID 7516—
ReactantTriethylamineHCID 8471—
ReactantDiethyl malonimidateHCID 73106—
SolventEthanolHCID 702—
Product1-Phenyl-1H-pyrazole-3,5-diamineHCID 23300065—

Reaction Conditions

Temperature95 °C

Reaction Steps

Triethylamine (6 ml) was added over 5 minutes to a stirred suspension of diethyl malonimidate dihydrochloride (5 g) in ethanol (50 ml). Phenylhydrazine (2.1 ml) was added, then the mixture was stirred at ambient temperature for 4 hours and at 95° C. for 30 minutes. The solvent was removed in vacuo, and the residue was partitioned between ethyl acetate (100 ml) and water (50 ml). The organic layer was separated, washed with water (50 ml), dried (MgSO4), and the solvent was removed in vacuo. The residue was purified by flash chromatography over silica using a 19:1 mixture of dichloromethane and methanol as eluant, appropriate fractions were combined, and the solvents were removed in vacuo to give 3,5-diamino-1-phenylpyrazole as a red-brown oil (0.76 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06114334
Source datasetuspto-grants-2000_09
ORD IDord-bf15116550614f689ee6e98a7444f0dd
Source noteuspto-grants-2000_09