HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 850973Generated: November 2, 2026
Methyl iodide → Ethyl 1-methyl-4-nitro-1H-pyrrole-2-carboxylate
https://huagongshe.com/reaction/850973
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Ethyl 4-Nitropyrrole-2-carboxylate | HCID 242169 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Ethyl 1-methyl-4-nitro-1H-pyrrole-2-carboxylate | HCID 10442704 | — |
Reaction Steps
A solution of 2.5 g. of sodium methoxide in 25 ml. of methanol is cooled to 10° C. and a mixture of 7.0 g. of ethyl 4-nitro-2-pyrrolecarboxylate in 15 ml. of methanol is added. After 10 minutes, 18.6 g. of methyl iodide is added. The dark-colored solution is warmed to 35° C. for 0.5 hours, then cooled and allowed to stir at room temperature for 16 hours. Chilling and filtration affords a solid which is collected by filtration and recrystallized from ethanol to yield the product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04382143 |
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| Source dataset | uspto-grants-1983_05 |
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| ORD ID | ord-ca9ef00cb187429cbafb22fc50d52524 |
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| Source note | uspto-grants-1983_05 |
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