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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
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 3-(Trifluoromethyl)benzaldehyde | HCID 67990 | — |
| 反応物 | 6-Bromo-2-methoxyquinoline | HCID 10657538 | — |
| 反応物 | Butyllithium | HCID 178418339 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | (+/-)-2-Methoxy-alpha-[3-(trifluoromethyl)phenyl]-6-quinoline methanol | HCID 54187627 | 66.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05922734 |
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| 出典データセット | uspto-grants-1999_07 |
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| ORD ID | ord-68c86418cf27496893ae3caa1b9f8bff |
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| 出典メモ | uspto-grants-1999_07 |
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