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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 384868Erstellt: 25. Oktober 2026

5-Methoxyindole-3-carbaldehyde → (5-methoxy-1H-indol-3-yl)methanol

https://huagongshe.com/reaction/384868

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt5-Methoxyindole-3-carbaldehydeHCID 82758—
EduktSodium borohydrideHCID 4311764—
LösungsmittelMethanolHCID 887—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelPotassium CarbonateHCID 11430—
Produkt(5-methoxy-1H-indol-3-yl)methanolHCID 425529370%

Reaktionsschritte

To a solution of sodium borohydride (2 grams, 0.05 mol) in methanol (15 ml), a solution of 5-methoxy-1H-indol-3-carboxaldehyde 2 (1 gram, 0.006 mol) dissolved in THF (20 ml) and methanol (15 ml) were combined and stirred at ambient temperature for 16 hours. The reaction was diluted with water and potassium carbonate (to saturation) and stirred to quench unreacted sodium borohydride. Diethyl ether was used to extract the product from the quenched solution. Following layers separation, the aqueous layer was further extracted (2×) with diethyl ether. The combined organic pats were dried over sodium sulfate and evaporated to dryness to yield a light colored solid 141 (736 mg, 70%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08367828B2
Quelldatensatzuspto-grants-2013_02
ORD IDord-d912c6b39a454f8fa6e28415445f49d8
Quellennotizuspto-grants-2013_02