Reaktionsgleichung
[H-].[H-].[H-].[H-].[Li+].[Al+3].[CH3:7][O:8][C:9]1[CH:17]=[C:16]2[C:12]([CH:13]=[C:14]([C:18](OC)=O)[NH:15]2)=[CH:11][CH:10]=1>O1CCOCC1>[CH3:7][O:8][C:9]1[CH:17]=[C:16]2[C:12]([CH:13]=[C:14]([CH3:18])[NH:15]2)=[CH:11][CH:10]=1Komponenten
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
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.
Aufarbeitung
- additionAfter the addition
- temperatureheated
- temperatureat reflux for 5 h
- temperatureAfter cooling to 0° C.
- customthe reaction is quenched by water (dropwise) and then 15% aqueous NaOH
- stirringAfter stirring at room temperature for 1 h
- filtrationthe mixture is filtered through Celite
- washThe solid is washed with a large amount of EtOAc
- washThe solvent is washed with brine
- dry with materialdried over Na2SO4
- customevaporated under vacuum
- customThe residue is purified by flash column chromatography on silica gel
Quellen und Nachweise
- ORD-Eintrag
- ord-abcfa7f9cad24899a50111778ccc839a
- Quelldatensatz
- uspto-grants-2011_01
- Patentnummer
- US07868037B2
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