HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1297353Generated: October 25, 2026
Methyl iodide → Methyl 1-methyl-1H-indole-3-carboxylate
https://huagongshe.com/reaction/1297353
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Methyl indole-3-carboxylate | HCID 589098 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 1-methyl-1H-indole-3-carboxylate | HCID 842006 | 96.3% |
Reaction Steps
NaH (60% dispersion in mineral oil, 8.56 g, 214.0 mmole) was added portionwise, allowing for gas evolution, to a solution of methyl 1H-indole-3-carboxylate (25.00 g, 142.7 mmole) in DMF (350 mL) at 0° C. When the NaH addition was complete, methyl iodide (44.4 mL, 713.5 mmole) was added at 0° C. The reaction was stirred at 0° C. for 15 minutes then at RT overnight. The reaction was diluted with water and extracted with ethyl acetate. The combined extracts were dried over K2CO3 and concentrated to afford the title compound (26.00 g, 96%) as an orange solid: MS (ES) m/e 190 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07250424B2 |
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| Source dataset | uspto-grants-2007_07 |
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| ORD ID | ord-57bb5209b7f64520afe125b22fee0872 |
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| Source note | uspto-grants-2007_07 |
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