HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2292231Generated: October 26, 2026
Benzene → Pyrazine, 2-methoxymethyl-5-methyl-, 4-oxide
https://huagongshe.com/reaction/2292231
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | 2-Hydroxymethyl-5-methylpyrazine-4-oxide | HCID 13023005 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Pyrazine, 2-methoxymethyl-5-methyl-, 4-oxide | HCID 3068148 | 152% |
Reaction Steps
2-Hydroxymethyl-5-methylpyrazine-4-oxide (3.5 g) was dissolved under stirring in a solution of 8 ml of thionyl chloride in 20 ml of dry benzene containing 0.5 g of ZnCl2, keeping the temperature below 30° C. The reaction mixture was cautiously warmed 3 hours at 60° C., then cooled to room temperature, and filtered. The solvent was evaporated under reduced pressure. The oily residue was dissolved in a solution of sodium methoxide in methyl alcohol, previously prepared dissolving 0.6 of sodium in 30 ml of methyl alcohol. After refluxing 4 hours, the reaction solution was cooled at room temperature, filtered and evaporated to dryness. The residue was taken up with water and repeatedly extracted with ethyl ether. The organic phase was washed with water, dried and the solvent was evaporated to dryness; the residue treated with pentane gave 2-methoxymethyl-5-methylpyrazine-4-oxide (1.5 g), m.p. 69°-72° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04801711 |
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| Source dataset | uspto-grants-1989_01 |
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| ORD ID | ord-d46cfbf90a1146b6838aee08baba915f |
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| Source note | uspto-grants-1989_01 |
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