HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 930458Generated: October 28, 2026
m-Chloroperbenzoic acid → 3-(Methoxycarbonyl)-2-methylpyrazine 1-oxide
https://huagongshe.com/reaction/930458
Participants
| Role | Name | HCID | Charge |
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| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | Methyl 3-methylpyrazine-2-carboxylate | HCID 13153469 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 3-(Methoxycarbonyl)-2-methylpyrazine 1-oxide | HCID 66665356 | — |
Reaction Steps
In a 1-L flask, the methyl 3-methylpyrazine-2-carboxylate (step 1, 16.08 g, 106 mmol) was suspended in CHCl3 (300 mL). 3-chlorobenzoperoxoic acid (Aldrich, 24.62 g, 143 mmol) was added. The reaction mixture was heated to 70° C. for 16 h. The reaction mixture was quenched with saturated NaHCO3 (200 mL). The layers were separated, and the aqueous layer was further extracted with DCM (2×100 mL). The combined organic layers were dried over MgSO4, and the filtrate was concentrated to afford the title compound. MS m/z=169 [M+H]+. Calculated for C7H8N2O3: 168.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09296734B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-0d3d63765fda4f76a07e41871055090e |
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| Source note | uspto-grants-2016_03 |
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