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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Sodium Sulfite | HCID 24437 | — |
| Reactant | 3-methylthio-11H-s-triazolo[3,4-b][3]benzazepine | HCID 21323406 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 3-methylsulfinyl-11H-s-triazolo[3,4-b][3]benzazepine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04150139 |
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| Source dataset | uspto-grants-1979_04 |
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| ORD ID | ord-22c04960834846a99b2bdb6b75cd2945 |
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| Source note | uspto-grants-1979_04 |
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