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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2300980Generated: October 30, 2026

Water → HCID 501121, compound

https://huagongshe.com/reaction/2300980

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPeracetic AcidHCID 6585—
ReactantSodium BisulfateHCID 516919—
ReactantHCID 22054754HCID 22054754—
SolventAcetic AcidHCID 176—
ProductHCID 501121HCID 501121—

Reaction Conditions

Temperature70 °C

Reaction Steps

To a mixture of 14.0 g (0.0426 mole) of 2-[[(4-chloro-3-nitrophenyl) methyl]sulfinyl]-pyridine-N-oxide in 35 ml of acetic acid was added 10.1 g of peracetic acid (40% in acetic acid) dropwise over one hour. The temperature of the reaction mixture rose to 27° C. before a water bath was placed on the flask to hold the temperature at 25° C. After addition, the mixture was heated to 70° C. for five hours. The mixture was cooled, and 20 ml additional acetic acid and solid sodium bisulfate and water were added to destroy the excess peracetic acid. The aqueous mixture was neutralized with potassium carbonate and chilled in an ice bath to precipitate an almost white solid. This solid was filtered off, washed with water, dried under vacuum overnight, and had a melting point of 162-164° C. Infrared and NMR spectra were both consistent with the proposed structure. The product was recrystallized from ethanol to give needle-like white crystals having a melting point of 168-170° C. C,H,N calculated for C12H9ClN2O5S: C=43.85%; H=2.76%; N=8.52%. Found: C=43.27% H=2.65%; N=8.21%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06498254B1
Source datasetuspto-grants-2002_12
ORD IDord-b16acdad71bd4de09d46a6a06f905c98
Source noteuspto-grants-2002_12