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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1620293Erstellt: 25. Oktober 2026

Sodium borohydride → (6-Methoxyquinolin-3-yl)methanol

https://huagongshe.com/reaction/1620293

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium borohydrideHCID 4311764—
Edukt6-Methoxyquinoline-3-carbaldehydeHCID 12329512—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(6-Methoxyquinolin-3-yl)methanolHCID 30466749%

Reaktionsschritte

To a stirred solution of 6-methoxyquinoline-3-carbaldehyde (1.00 g, 5.3 mmol) in THF (50 mL) in a 100 mL round-bottomed flask equipped with a magnetic stirrer was added NaBH4 (0.20 g, 5.3 mmol) and the mixture was stirred overnight at RT then cooled in an ice bath before quenching by addition of a 1 N aq. HCl solution (12 mL). After stirring for 15 min at RT, the mixture was basified to pH=9 with a 2 N aq. NaOH solution. THF was removed at 40° C. under vacuum and the solution was extracted with CH2Cl2 (200 mL), washed with brine (20 mL), dried over Na2SO4, filtered, and concentrated under vacuum. Purification by column chromatography (SiO2, eluent cyclohexane:EtOAc=100:0 to 0:100) gave (6-methoxyquinolin-3-yl)methanol SLA 47088A as a yellow solid (0.49 g, 49% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08772316B2
Quelldatensatzuspto-grants-2014_07
ORD IDord-77b919bd3e704a9498fde23658395d54
Quellennotizuspto-grants-2014_07