HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1015441Generated: October 30, 2026
Methyl iodide → Methyl 3-(methoxymethyl)-1H-indole-5-carboxylate
https://huagongshe.com/reaction/1015441
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Methyl 3-(hydroxymethyl)-1H-indole-5-carboxylate | HCID 67300394 | — |
| Catalyst | Silver(II) oxide | HCID 92152 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Methyl 3-(methoxymethyl)-1H-indole-5-carboxylate | HCID 67300506 | — |
Reaction Steps
A 327 mg portion of methyl 3-(hydroxymethyl)-1H-indole-5-carboxylate was dissolved in 9 ml of acetonitrile, mixed with 385 mg of silver oxide and 3.6 ml of methyl iodide and stirred at 80° C. for 5 hours. A 385 mg portion of silver oxide was further added thereto and stirred overnight at 80° C. A 385 mg portion of silver oxide and 3.6 ml of methyl iodide were further added thereto and stirred at 80° C. for 9 hours. After cooling to room temperature, the insoluble matter was removed, the solvent was evaporated, and then the residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:6 to 1:5 to 1:4) to obtain 143 mg of methyl 3-(methoxymethyl)-1H-indole-5-carboxylate as a pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07985764B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-71d787d2a80b42b096f37d813ecec770 |
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| Source note | uspto-grants-2011_07 |
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