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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 252512Generated: October 25, 2026

Methyl-6-methoxy-2-indolecarboxylate → 6-methoxy-2-methyl-1H-indole

https://huagongshe.com/reaction/252512

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl-6-methoxy-2-indolecarboxylateHCID 688173—
ReactantAluminium lithium hydrideHCID 21226445—
Solvent1,4-DioxaneHCID 31275—
Product6-methoxy-2-methyl-1H-indoleHCID 1084470961%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07868037B2
Source datasetuspto-grants-2011_01
ORD IDord-abcfa7f9cad24899a50111778ccc839a
Source noteuspto-grants-2011_01