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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methylglyoxal | HCID 880 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 2-Aminomalononitrile 4-toluenesulfonate | HCID 18796971 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 3-methoxy-5-methylpyrazine-2-carboxylate | HCID 21702987 | 27% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06235905B1 |
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| Source dataset | uspto-grants-2001_05 |
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| ORD ID | ord-51fd19501f9b403d87cd1b28889fd240 |
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| Source note | uspto-grants-2001_05 |
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