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HRID 581998作成日:2026年10月25日

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

https://huagongshe.com/reaction/581998

反応式

関与物質

役割名称HCID仕込み量
反応物3-(Trifluoromethyl)benzaldehydeHCID 67990—
反応物6-Bromo-2-methoxyquinolineHCID 10657538—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物(+/-)-2-Methoxy-alpha-[3-(trifluoromethyl)phenyl]-6-quinoline methanolHCID 5418762766.1%

反応条件

温度-78 °C

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05922734
出典データセットuspto-grants-1999_07
ORD IDord-68c86418cf27496893ae3caa1b9f8bff
出典メモuspto-grants-1999_07