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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 26522Generated: October 26, 2026

Hydrogen Peroxide → 3-methylsulfinyl-11H-s-triazolo[3,4-b][3]benzazepine

https://huagongshe.com/reaction/26522

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantSulfuric AcidHCID 1118—
ReactantSodium SulfiteHCID 24437—
Reactant3-methylthio-11H-s-triazolo[3,4-b][3]benzazepineHCID 21323406—
SolventAcetic AcidHCID 176—
Product3-methylsulfinyl-11H-s-triazolo[3,4-b][3]benzazepineHCID 21323529—

Reaction Steps

To 0.230 g of 3-methylthio-11H-s-triazolo[3,4-b][3]benzazepine in 3 ml of acetic acid was added 0.2 ml of concentrated sulfuric acid and, under ice-cooling, 0.3 ml of a 30% aqueous solution of hydrogen peroxide was added dropwise. The mixture was allowed to stand at 3°-5° C. for 7 hours, at the end of which time an aqueous solution of sodium sulfite was added to the mixture to decompose the excess hydrogen peroxide. The solvent was evaporated off and the residue was diluted with water. The crystals were collected by filtration. By the above procedure was obtained 3-methylsulfinyl-11H-s-triazolo[3,4-b][3]benzazepine as crystals. Recrystallization from methanol yielded colorless needles, m.p. 176°-177° C. Based on infrared absorption spectrum and other data, this compound was identified with the compound obtained in Example 17.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04150139
Source datasetuspto-grants-1979_04
ORD IDord-22c04960834846a99b2bdb6b75cd2945
Source noteuspto-grants-1979_04