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HRID 30755作成日:2026年10月25日

Cesium fluoride → 4'-(2-Hydroxyethoxy)-3',5'-dimethylbiphenyl-4-carboxylic acid

https://huagongshe.com/reaction/30755

反応式

関与物質

役割名称HCID仕込み量
反応物Cesium fluorideHCID 25953—
反応物1,4-DioxaneHCID 31275—
反応物4-Carboxyphenylboronic AcidHCID 312183—
反応物2-(4-Bromo-2,6-dimethylphenoxy)ethanolHCID 53707443—
触媒HCID 178418397HCID 178418397—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
溶媒Ethyl AcetateHCID 8857—
生成物4'-(2-Hydroxyethoxy)-3',5'-dimethylbiphenyl-4-carboxylic acidHCID 2309073138.2%

反応条件

温度90 °C

反応手順

A mixture of 2-(4-bromo-2,6-dimethylphenoxy)ethanol (0.65 g), 4-carboxyphenylboronic acid (0.87 g), tetrakis(triphenylphosphine)palladium(0) (0.15 g), cesium fluoride (2.40 g), 1,4-dioxane (7.5 mL), ethanol (2.5 mL) and water (1.5 mL) was stirred at 90° C. overnight under an atmosphere of argon. Water and ethyl acetate were added to the reaction mixture. The organic layer was separated, washed with water and brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (eluent:ethyl acetate/n-hexane=1/1-2/1) to afford the title compound (0.29 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07423185B2
出典データセットuspto-grants-2008_09
ORD IDord-29c629dfd82e403abf56ff372f921911
出典メモuspto-grants-2008_09