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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1978140Generated: October 25, 2026

Acetic Acid → Methyl 3-methoxy-5-methylpyrazine-2-carboxylate

https://huagongshe.com/reaction/1978140

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHydrochloric AcidHCID 313—
ReactantMethylglyoxalHCID 880—
ReactantSodium MethoxideHCID 10942334—
Reactant2-Aminomalononitrile 4-toluenesulfonateHCID 18796971—
SolventMethanolHCID 887—
ProductMethyl 3-methoxy-5-methylpyrazine-2-carboxylateHCID 2170298727%

Reaction Conditions

Temperature2 °C

Reaction Steps

Under argon, 5 g (19.3 mmol) of 2-aminomalononitrile-4-toluenesulfonate was initially charged in 50 g of methanol. 4.09 g (22.7 mmol) of sodium methoxide solution (30%) was added and the mixture was stirred at 2° C. for 2 hours. After neutralization with 0.204 g (3.4 mmol) of acetic acid, 3.6 g (19.9 mmol) of methylglyoxal solution (40%) was added. The mixture was stirred at 40° C. for 2 hours and then, at 20° C., 9.2 g (80 mmol) of hydrochloric acid (32%) was added and the mixture was stirred at 20° C. for 6 hours. The solvent was distilled off and the methyl 3-methoxy-5-methylpyrazine-2-carboxylate was extracted with methylene chloride. This gave 1 g of methyl 3-methoxy-5-methylpyrazine-2-carboxylate. The yield was 27 percent Other data concerning the title product was:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06235905B1
Source datasetuspto-grants-2001_05
ORD IDord-51fd19501f9b403d87cd1b28889fd240
Source noteuspto-grants-2001_05