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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1369075Generated: October 31, 2026

Hydrogen Peroxide → HCID 11176292, compound

https://huagongshe.com/reaction/1369075

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantSodium SulfiteHCID 24437—
ReactantHCID 11429986HCID 11429986—
SolventAcetic AcidHCID 176—
ProductHCID 11176292HCID 11176292—

Reaction Conditions

Temperature50 °C

Reaction Steps

To crude methyl 3-[2-nitro-4-iodo-6-(trifluoromethyl)phenyl]-2-oxo-propanoate prepared above (40.98 g) in AcOH (750 mL) was added aqueous 30% H2O2 solution (266 mL) followed by 70% HClO4 (41 mL). The resulting mixture was stirred at 50° C. (bath temperature) for 4.5 hours. The solution was cooled and solid Na2SO3 (100 g) was added. The solvent was then removed in vacuo. The resulting orange solid was suspended in EtOAc (500 mL) and washed with H2O (300 mL). The organic phase was then extracted with aqueous saturated NaHCO3:aqueous 2N NaOH (6:1, 600 mL) followed by aqueous saturated NaHCO3 (200 mL). The aqueous extracts were combined and cooled in an ice-water bath. The solution was then acidified with aqueous 35% HCl. The resulting solid was isolated by filtration and dried to give the title compound as a yellow solid (7.086 g). The organic phase was then re-extracted with aqueous saturated NaHCO3 (6×50 mL). The extracts were combined and cooled in an ice-water bath, and then acidified with aqueous 35% HCl. The resulting solid was isolated by filtration and dried to give the title compound as a yellow solid (6.896 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06576656B1
Source datasetuspto-grants-2003_06
ORD IDord-b8428b949ddb4ace9364b788a28aa71c
Source noteuspto-grants-2003_06