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HRID 50163作成日:2026年10月24日

Sodium Hydroxide → 6-Bromo4-(3-ethoxy-phenyl)-2-methoxy-quinoline

https://huagongshe.com/ja/reaction/50163

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium HydroxideHCID 14798—
反応物Oxonium, trimethyl-, tetrafluoroborate(1-) (1:1)HCID 2735153—
反応物6-Bromo4-(3-ethoxy-phenyl)-1h-quinolin-2-oneHCID 22465443—
溶媒1,1-DichloroethaneHCID 6365—
生成物6-Bromo4-(3-ethoxy-phenyl)-2-methoxy-quinolineHCID 2246541958.2%

反応手順

To a suspension of 6-bromo-4-(3-ethoxy-phenyl)-1H-quinolin-2-one (7.4 g, 21.5 mmol) in 60 ml dichloroethane was added trimethyloxonium tetrafluoroborate (BF4OMe3, 3.66 g, 24.7 mmol). The resulting mixture was stirred at ambient temperature overnight. After cooling to 0° C., was added 60 ml of 10% aqueous NaOH dropwise. The reaction mixture was stirred for another six hours at ambient temperature. It was then partitioned between dichloromethane and water. The organic layer was washed brine, dried over MgSO4, filtered and concentrated under vacuum to give an off-white solid. The solid was chromatographed on flash silica gel eluting with dichoromethane to yield the titled compound of 23A as a white solid (4.48 g, 58% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06710209B2
出典データセットuspto-grants-2004_03
ORD IDord-8cb0a23cb9cb4214a6753163d2276bc8
出典メモuspto-grants-2004_03