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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1576103Generated: November 2, 2026

2,5-Hexanedione → 89151-79-1

https://huagongshe.com/reaction/1576103

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,5-HexanedioneHCID 8035—
ReactantPotassium HydroxideHCID 14797—
ReactantMaleic AcidHCID 444266—
Reactant39889-17-3HCID 12221230—
SolventBenzeneHCID 241—
SolventEthanolHCID 702—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
Product89151-79-1HCID 24838949—

Reaction Steps

To a boiling solution of 8.63 g. (0.0756 mole) of 2,5-hexanedione in 50 ml. of absolute ethanol, a solution of 14 g. (0.0614 mole) of 2-hydrazino-4,5-dihydro-1H-imidazole hydroiodide and 3.47 g. (0.0620 mole) of potassium hydroxide in 120 ml. of absolute ethanol and 60 ml. of anhydrous benzene is quickly added. The mixture is stirred under reflux for 30 minutes and at room temperature for 12 hours. The potassium iodide which forms is cast off by filtration, then the mixture is concentrated to small volume by evaporating off the solvent. A residue is obtained which is dissolved with methylene chloride. To the obtained solution an ether solution of maleic acid is added and a precipitate readily forms, which is recrystallized two times from absolute ethanol. Yield 1.3 g. M.p. 177°-8°C. The free base melts at 192°-3°C (from methanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03979408
Source datasetuspto-grants-1976_09
ORD IDord-39d35ffd23a9428b9ba068295a953a2d
Source noteuspto-grants-1976_09