HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2107322Generated: October 30, 2026
m-Chloroperbenzoic acid → 3-Methyl-2-(2-pyridylmethylsulfinyl)quinoxaline
https://huagongshe.com/reaction/2107322
Participants
| Role | Name | HCID | Charge |
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| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 14052175 | HCID 14052175 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 3-Methyl-2-(2-pyridylmethylsulfinyl)quinoxaline | HCID 14052180 | 67.2% |
Reaction Steps
In a mixture of 36 ml of chloroform and 18 ml of methanol was dissolved 2.6 g of 3-methyl-2-(2-pyridylmethylthio)quinoxaline hydrochloride. To the chilled solution kept at a temperature of lower than 0° C. (temperature of solution) was added 1.77 g of m-chloroperbenzoic acid (purity 70%). After the reaction was complete, chloroform and saturated aqueous NaHCO3 solution were added to the reaction mixture under chilling. The organic layer was separated and dried over sodium sulfate. The sodium sulfate was then removed by filtration, and the solvent was evaporated under reduced pressure from the filtrate. The residue was purified by silica gel column chromatography (chloroform/methanol), and recrystallized from ethyl/hexane to give 1.63 g of 3-methyl-2-(2-pyridylmethylsulfinyl)quinoxaline as an orange crystalline powder, m.p. 85°-88° C. (decompn.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04933458 |
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| Source dataset | uspto-grants-1990_06 |
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| ORD ID | ord-54d9b0005925471ca2437c82105f97f3 |
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| Source note | uspto-grants-1990_06 |
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