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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2166983Generated: October 30, 2026

Hydrogen Peroxide → HCID 131732894, compound

https://huagongshe.com/reaction/2166983

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantSodium CarbonateHCID 10340—
ReactantSodium ThiosulfateHCID 24477—
ReactantHCID 121292342HCID 121292342—
CatalystTetrabutylammonium BromideHCID 74236—
SolventMethanolHCID 887—
ProductHCID 131732894HCID 131732894889.9%

Reaction Steps

To a methanol solution (140 ml) of 29.0 g (137 mM) of 3-amino-2,3-bis(isopropoxyimino)propionitrile were added, at room temperature, 47 g (415 mM) of a 30% aqueous hydrogen peroxide solution, 1.5 g (15 mM) of sodium carbonate and 2.3 g (7.1 mM) of tetrabutylammonium bromide. Stirring was conducted at room temperature for 4 hours. Since the raw materials remained, further 24 g (212 mM) of a 30% aqueous hydrogen peroxide solution was added, followed by stirring at room temperature for 3 hours. Excessive hydrogen peroxide was treated with an aqueous sodium thiosulfate solution. The solvent was distilled off under reduced pressure. Water was added to the resulting residue, followed by extraction with ethyl acetate. The organic layer obtained was washed with a saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, and filtered to remove inorganic matter. The solvent was distilled off under reduced pressure. The crystal obtained was washed with a 1:2 mixed solution of diisopropyl ether and n-hexane to obtain 29.0 g (yield: 92%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09044013B2
Source datasetuspto-grants-2015_06
ORD IDord-a140ce6aff4d4f5a827335f299bf6bd3
Source noteuspto-grants-2015_06