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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 576957Erstellt: 25. Oktober 2026

3-Quinolinecarboxaldehyde → (Quinolin-3-yl)methanol

https://huagongshe.com/reaction/576957

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-QuinolinecarboxaldehydeHCID 83641—
EduktSodium borohydrideHCID 4311764—
LösungsmittelEthanolHCID 702—
Produkt(Quinolin-3-yl)methanolHCID 12662983—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

In a 250 mL round bottom flask, quinoline-3-carbaldehyde (1.57 g, 10 mmol) was dissolved anhydrous ethanol (20 mL). The solution was cooled to 0° C. under nitrogen. NaBH4 (420 mg, 11 mmol) was added in one portion. The mixture was stirred at room temperature for 2 hours, and quenched by addition of water (3 mL). Na2SO4 (15 g) was added. After 10 minutes, the mixture was filtered. The filtrate was evaporated to provide quinolin-3-ylmethanol.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09040538B2
Quelldatensatzuspto-grants-2015_05
ORD IDord-5cb8498e4d874eee874d8ceafcc87088
Quellennotizuspto-grants-2015_05