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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantMethyl 3-methylpyrazine-2-carboxylateHCID 13153469—
SolventChloroformHCID 6212—
Product3-(Methoxycarbonyl)-2-methylpyrazine 1-oxideHCID 66665356—

Reaction Conditions

Temperature70 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09296734B2
Source datasetuspto-grants-2016_03
ORD IDord-0d3d63765fda4f76a07e41871055090e
Source noteuspto-grants-2016_03