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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 26519Generated: October 29, 2026

Acetic Acid → HCID 21323360, compound

https://huagongshe.com/reaction/26519

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHydrogen PeroxideHCID 784—
ReactantSulfuric AcidHCID 1118—
ReactantSodium SulfiteHCID 24437—
Reactant8-methyl-3-methylthio-11H-s-triazolo[3,4-b][3]benzazepineHCID 21323337—
ProductHCID 21323360HCID 21323360—

Reaction Steps

To a solution of 6.1 g of 8-methyl-3-methylthio-11H-s-triazolo[3,4-b][3]benzazepine in 75 ml of acetic acid was added 5.0 ml of concentrated sulfuric acid and under ice-cooling and stirring, 12.5 ml of 30% H2O2 was added dropwise. After stirring the mixture for 10 minutes at room temperature, it was heated on a water bath at 60°-65° C. for 2 hours. After ice-cooling, an aqueous solution of sodium sulfite was added to decompose the excess hydrogen peroxide. The solvent was evaporated off and, following addition of water, the residue was neutralized with concentrated aqueous ammonia, again under ice-cooling, and extracted with chloroform. The chloroform layer was washed with water and dried over Na2SO4. The solvent was evaporated off and the residue was treated with ether. By the above procedure was obtained 8-methyl-3-methylsulfonyl-11H-s-triazolo[3,4-b][3]benzazepine as crystals. Recrystallization from ethanol yielded colorless needles melting at 152°-153° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04150139
Source datasetuspto-grants-1979_04
ORD IDord-0a922bacd59e439491327d8fca27fcba
Source noteuspto-grants-1979_04