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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1883203Erstellt: 26. Oktober 2026

Ethyl Acetate → 5-Methoxy-1H-indole-2-carbaldehyde

https://huagongshe.com/reaction/1883203

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl AcetateHCID 8857—
Edukt5-Methoxyindole-2-carboxylic acidHCID 20401—
EduktAluminium lithium hydrideHCID 21226445—
KatalysatorManganese dioxideHCID 14801—
LösungsmittelHydrochloric AcidHCID 313—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt5-Methoxy-1H-indole-2-carbaldehydeHCID 82645636%

Reaktionsschritte

Under nitrogen atmosphere, to a solution of 5-methoxyindole-2-carboxylic acid (1.00 g) in Et2O (40 mL) was added LiAlH4 (280 mg) at 0° C., and the mixture was stirred under reflux for 3 hours. The mixture was treated with ethyl acetate, diluted with an aqueous hydrochloric acid solution, and extracted with ethyl acetate. The mixture was concentrated to give a crude alcohol compound (840 mg, 91%), which was dissolved in THF (10 mL), and stirred with MnO2 (4.20 g) at room temperature for 5 hours. The mixture was filtered on celite, and the filtrate was concentrated, and the residue was purified by silica gel column chromatography to give 5-methoxyindole-2-carbaldehyde (300 mg, 36%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06759429B2
Quelldatensatzuspto-grants-2004_07
ORD IDord-3f1376d864da42359218ce88038a9077
Quellennotizuspto-grants-2004_07