HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1090319Generated: November 4, 2026
Hydrogen Peroxide → HCID 178527208, compound
https://huagongshe.com/reaction/1090319
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Selenium Dioxide | HCID 24007 | — |
| Reactant | HCID 178506164 | HCID 178506164 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178527208 | HCID 178527208 | — |
Reaction Steps
2-[[[3-(Trifluoromethyl)phenyl]methyl]thio]-1H-imidazo[4,5-c]pyridine (0.91 g, 0.0029 mol) was dissolved in 10 mL of ethanol. An oxidizing solution was prepared by dissolving 0.32 g (0.0029 mol) of selenium dioxide in 17 mL of ethanol by heating and adding 0.33 g (0.0029 mol) of 30% hydrogen peroxide and 0.25 mL of water. The oxidizing solution was added dropwise to the sulfide solution and the reaction mixture was stirred overnight at room temperature. Water (20 mL) was added to the reaction mixture which was then extracted with chloroform (3×25 mL). The combined organic layers were dried over magnesium sulfate, filtered and evaporated to dryness. The residue amounted to 0.65 g. Purification by HPLC gave a product which on recrystallization from ethanol had a m.p. 194°-197° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05081253 |
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| Source dataset | uspto-grants-1992_01 |
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| ORD ID | ord-eff100033a19414b9633a25ab9df90d8 |
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| Source note | uspto-grants-1992_01 |
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