HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 627702Generated: October 30, 2026
m-Chloroperbenzoic acid → 3-(Methoxycarbonyl)-2-methylpyrazine 1-oxide
https://huagongshe.com/reaction/627702
Participants
| Role | Name | HCID | Charge |
|---|
| 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).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09309263B2 |
|---|
| Source dataset | uspto-grants-2016_04 |
|---|
| ORD ID | ord-64d1fd1cfcd24489b7f41b917099fe2c |
|---|
| Source note | uspto-grants-2016_04 |
|---|