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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 627688Generated: October 30, 2026

Trifluoroacetic anhydride → HCID 86728142, compound

https://huagongshe.com/reaction/627688

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantCarbamide PeroxideHCID 31294—
ReactantMethyl 3-methylpyrazine-2-carboxylateHCID 13153469—
Reactant3-(Methoxycarbonyl)-2-methylpyrazine 1-oxideHCID 66665356—
SolventDichloromethaneHCID 6344—
ProductHCID 86728142HCID 8672814251.7%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09309263B2
Source datasetuspto-grants-2016_04
ORD IDord-ac510f0b48b345f09c0b4d7c7e7391db
Source noteuspto-grants-2016_04