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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 581998Erstellt: 24. Oktober 2026

3-(Trifluoromethyl)benzaldehyde → (+/-)-2-Methoxy-alpha-[3-(trifluoromethyl)phenyl]-6-quinoline methanol

https://huagongshe.com/de/reaction/581998

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-(Trifluoromethyl)benzaldehydeHCID 67990—
Edukt6-Bromo-2-methoxyquinolineHCID 10657538—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(+/-)-2-Methoxy-alpha-[3-(trifluoromethyl)phenyl]-6-quinoline methanolHCID 5418762766,1%

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

Butyllithium (12.5 ml) was added dropwise at -78° C. to a solution of 6-bromo-2-methoxyquinoline (4 g) in tetrahydrofuran (160 ml). After complete addition the mixture was stirred at -78° C. for 15 minutes. A solution of 3-(trifluoromethyl)-benzaldehyde (3.51 g) in tetrahydrofuran (40 ml) was added dropwise and the mixture was stirred at -78° C. for 30 minutes, then quenched with water (50 ml) and extracted with ethylacetate. The organic layer was separated, washed with brine, dried over MgSO4, filtered and the solvent was evaporated. The residue was purified by column chromatography over silica gel (eluent: CH2Cl2 /CH3OH 97/3). The pure fractions were collected and the solvent was evaporated, yielding 3.7 g (66%) of (±)-2-methoxy-α-[3-(trifluoromethyl)phenyl]-6- quinoline methanol (intermediate 28).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05922734
Quelldatensatzuspto-grants-1999_07
ORD IDord-68c86418cf27496893ae3caa1b9f8bff
Quellennotizuspto-grants-1999_07