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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1699481Generated: October 29, 2026

Hydrogen Peroxide → HCID 9862505, compound

https://huagongshe.com/reaction/1699481

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantSulfuric AcidHCID 1118—
ReactantSodium SulfiteHCID 24437—
ReactantHCID 10892558HCID 10892558—
ReactantHCID 10924734HCID 10924734—
ReactantSodium HypochloriteHCID 23665760—
ReactantSodium ChloriteHCID 23668197—
CatalystTempoHCID 2724126—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductHCID 9862505HCID 986250551.7%

Reaction Steps

The compound (4) (51.26 g, 155 mmol) prepared in above (3) was dissolved in acetonitrile (1.54 L), and TEMPO (2,2, 6,6-tetramethylpiperidine-1-oxyl, 250 mg, 0.01 eq.) was added thereto. To the mixture was added dropwise 0.81 N aqueous sodium hypochlorite, which had been prepared by diluting 1.63 N aqueous sodium hypochlorite (150ml) with water (75 ml), adjusting pH 8.6 with 1 N sulfuric acid, and adjusting the total volume to 300 ml, over 15 minutes, while maintaining the inner temperature between −1° C. and 8° C. After stirring for 25 minutes at this temperature, 1 N aqueous sodium sulfite (32 ml) was added. Subsequently, 79% sodium chlorite (27.48 g, 240 mmol) and 31% aqueous hydrogen peroxide (23.26 g, 212 mmol) were added under ice-cooling. The cooling bath was removed and the mixture was stirred for 2 hours. The reaction was diluted with water (1.5 L), adjusted to pH 3 with 1 N hydrochloric acid and the deposited crystals were filtered, and washed twice with water (200 ml), acetonitrile (50 ml) to provide 32.4 g of crude crystals. The crude crystals (32.4 g) were suspended in acetonitrile (224 ml), refluxed for 15 minutes and cooled on ice. The crystals were filtered and washed with acetonitrile (65 ml) to provide 26.79 g of the title compound (6). Yield: 51.7%, mp 202-203° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06346628B1
Source datasetuspto-grants-2002_02
ORD IDord-b3fb5e9029f34a3793328c080d8b6ef3
Source noteuspto-grants-2002_02