HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 225862Generated: October 27, 2026
Methyl iodide → methyl 4-methoxy-1-methyl-1H-indole-2-carboxylate
https://huagongshe.com/reaction/225862
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | methyl 4-methoxy-1H-indole-2-carboxylate | HCID 688172 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | methyl 4-methoxy-1-methyl-1H-indole-2-carboxylate | HCID 4777904 | 96.5% |
Reaction Steps
NaH (60% dispersion in mineral oil, 03 g, 7.3 mmole) was washed with hexane then suspended in anhydrous DMF (16 mL). The mixture was cooled to 0° C. and methyl 4-methoxy-1H-indol-2-carboxylate (1.0 g, 4.87 mmole) was added. The mixture was stirred under argon for 10 min, then MeI (1.3 mL, 20 mmole) was added, and the thick slurry was stirred at RT for 2.5 hr. The reaction was quenched with 10% NH4Cl (2 mL) and concentrated. The residue was partitioned between H2O and Et2O, and the organic layer was dried over MgSO4 and concentrated to yield the title compound (1.03 g, 96%) as a white solid: MS (ES) m/e 220.2 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07557125B2 |
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| Source dataset | uspto-grants-2009_07 |
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| ORD ID | ord-dc808ffbce5b4b6bad862c0ffa2258ee |
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| Source note | uspto-grants-2009_07 |
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