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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 393008Erstellt: 24. Oktober 2026

Ethyl Acetate → 1H-indol-4-ylmethanol

https://huagongshe.com/de/reaction/393008

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl AcetateHCID 8857—
Eduktmethyl 1H-indole-4-carboxylateHCID 2733668—
EduktPotassium sodium tartarateHCID 9855836—
EduktDiisobutylaluminumhydrideHCID 21225700—
LösungsmittelDiethyl EtherHCID 3283—
Produkt1H-indol-4-ylmethanolHCID 2773457101,5%

Reaktionsbedingungen

Temperatur-70 °C

Reaktionsschritte

Diisobutylaluminum hydride (1 M in toluene; 1.3 mL, 1.3 mmol) was added to a solution of 1H-indole-4-carboxylic acid, methyl ester (85 mg, 0.49 mmol) in ether (1.6 mL) at −70° C. The solution was allowed to stir at −70° C. for 1 h, then at room temperature for 1 h. Ethyl acetate (20 mL) was added, and the solution was stirred with an aqueous solution of potassium sodium tartrate (30% w/v; 20 mL) for 30 min. The layers were separated and the aqueous layer was extracted with ethyl acetate. The combined organic layers were dried (MgSO4), filtered, evaporated, and dried under high vacuum to give 1H-indole-4-methanol (73.2 mg, quantitative yield) which was used in the next step without further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06803384B2
Quelldatensatzuspto-grants-2004_10
ORD IDord-43b8b6bb80274100a5fdb0ce735ba707
Quellennotizuspto-grants-2004_10