HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 502138Generated: October 25, 2026
Methyl-6-methoxy-2-indolecarboxylate → 6-methoxy-2-methyl-1H-indole
https://huagongshe.com/reaction/502138
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl-6-methoxy-2-indolecarboxylate | HCID 688173 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 6-methoxy-2-methyl-1H-indole | HCID 10844709 | 61% |
Reaction Steps
To a suspension of LiAlH4 (7.6 g, 0.2 mol) in dioxane (100 mL) is added dropwise a solution of methyl 6-methoxy-1H-indole-2-carboxylate (8.2 g, 0.04 mol) in dioxane (50 mL) at 0° C. After the addition, the mixture is stirred at room temperature for 1 h and then heated at reflux for 5 h. After cooling to 0° C., the reaction is quenched by water (dropwise) and then 15% aqueous NaOH. After stirring at room temperature for 1 h, the mixture is filtered through Celite. The solid is washed with a large amount of EtOAc. The solvent is washed with brine, dried over Na2SO4 and evaporated under vacuum. The residue is purified by flash column chromatography on silica gel using EtOAc/petroleum ether (1/5) as eluent to yield 61% of 6-methoxy-2-methyl-1H-indole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07772271B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-88d886f9e40848cf9a77ef484c93c214 |
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| Source note | uspto-grants-2010_08 |
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