HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 627688Generated: October 30, 2026
Trifluoroacetic anhydride → HCID 86728142, compound
https://huagongshe.com/reaction/627688
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | Carbamide Peroxide | HCID 31294 | — |
| Reactant | Methyl 3-methylpyrazine-2-carboxylate | HCID 13153469 | — |
| Reactant | 3-(Methoxycarbonyl)-2-methylpyrazine 1-oxide | HCID 66665356 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86728142 | HCID 86728142 | 51.7% |
Reaction Steps
To a solution of methyl 3-methylpyrazine-2-carboxylate (9.1 g, 59.8 mmol) in DCM (100 mL) at 0° C., was added urea hydrogen peroxide adduct, 97% (7.81 g, 83 mmol) and trifluoroacetic acid anhydride (10.8 ml, 78 mmol) dropwise. The resulting mixture was stirred at 0° C. for 1 h, and at room temperature for 18 h. The reaction was diluted with DCM and quenched with saturated Na2SO3 solution; the aqueous layer was back-extracted with DCM. The combined organic extracts were dried (MgSO4), filtered and concentrated in vacuo. The crude mixture was purified with ISCO (20% to 80% EtOAc/Hexanes) to afford a mixture of products: 2-(methoxycarbonyl)-3-methylpyrazine 1-oxide (5.2 g, 51.7% yield) and 3-(methoxycarbonyl)-2-methylpyrazine 1-oxide. The mixture was taken to next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09309263B2 |
|---|
| Source dataset | uspto-grants-2016_04 |
|---|
| ORD ID | ord-ac510f0b48b345f09c0b4d7c7e7391db |
|---|
| Source note | uspto-grants-2016_04 |
|---|