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HRID 857597作成日:2026年10月25日

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

https://huagongshe.com/reaction/857597

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US07145047B2
出典データセットuspto-grants-2006_12
ORD IDord-6d57c44af68c45c89effe9f8ba284733
出典メモuspto-grants-2006_12