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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 351601Erstellt: 24. Oktober 2026

2-Quinolinecarboxaldehyde → 2-Quinolinemethanol

https://huagongshe.com/de/reaction/351601

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-QuinolinecarboxaldehydeHCID 79619—
EduktSodium borohydrideHCID 4311764—
LösungsmittelEthanolHCID 702—
Produkt2-QuinolinemethanolHCID 73196—
Produkt(1,2,3,4-Tetrahydroquinolin-2-yl)methanolHCID 15052240—

Reaktionsschritte

Sodium borohydride (21.7 g, 0.57 mol) was added in portions to a solution of quinoline-2-carboxaldehyde (30 g, 0.191 mol) in ethanol (300 mL) at 0° C. The reaction mixture was warmed to room temperature, stirred at room temperature for 2 hrs, and quenched by water. Volatiles were removed under reduced pressure and the residue dissolved in ethyl acetate, washed with water and saturated aqueous sodium chloride, dried over sodium sulfate, and concentrated under reduced pressure. The residue was subjected to silica gel chromatography. Fractions containing product were combined and concentrated under reduced pressure to provide the desired compound and 2-(hydroxymethyl)quinoline. A solution of the recovered 2-(hydroxymethyl)quinoline in ethanol (250 mL) and tetrahydrofuran (250 mL) was hydrogenated at 60 psi in the presence of 5% platinum on carbon at 40° C. for 48 hours. The reaction mixture was filtered and the filtrate concentrated under reduced pressure to provide the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06743785B2
Quelldatensatzuspto-grants-2004_06
ORD IDord-f6f7b93775e143ccb92bc7a447b47d8b
Quellennotizuspto-grants-2004_06