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HRID 992187作成日:2026年10月24日

Toluene → 6-(3,4-Difluorophenyl)-2-naphthol

https://huagongshe.com/ja/reaction/992187

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物Potassium CarbonateHCID 11430—
反応物6-Bromo-2-naphthalenolHCID 27144—
反応物3,4-Difluorophenylboric acidHCID 21869672—
触媒HCID 178418397HCID 178418397—
溶媒EthanolHCID 702—
生成物6-(3,4-Difluorophenyl)-2-naphtholHCID 2187082088.1%

反応手順

To 25.0 g of 6-bromo-2-naphthol and 22.0 g of 3,4-difluorophenylboric acid were added 100 ml of toluene, 50 ml of ethanol, 50 ml of a 2 N aqueous solution of potassium carbonate and 1.3 g of tetrakis(triphenylphosphine)palladium (0). The reaction mixture was heated under reflux for 3 hours. The reaction solution was then allowed to cool to room temperature. The resulting organic phase was separated, washed with water and saturated brine, and then dried over anhydrous sodium sulfate. The solvent was then distilled off. The residue was purified through silica gel column chromatography (dichloromethane) to obtain 25.3 g of 6-(3,4-difluorophenyl)-2-naphthol.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06468607B1
出典データセットuspto-grants-2002_10
ORD IDord-49778d7a77264410acd17cf44f6a8f6c
出典メモuspto-grants-2002_10