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HRID 2170208作成日:2026年10月26日

Bromide ion → (2-(2,4-Difluorophenoxy)-5-(trifluoromethyl)phenyl)boronic acid

https://huagongshe.com/reaction/2170208

反応式

関与物質

役割名称HCID仕込み量
反応物Bromide ionHCID 259—
反応物Trimethyl borateHCID 8470—
反応物MagnesiumHCID 5462224—
反応物2-Bromo-1-(2,4-difluorophenoxy)-4-(trifluoromethyl)benzeneHCID 89656289—
溶媒TetrahydrofuranHCID 8028—
生成物(2-(2,4-Difluorophenoxy)-5-(trifluoromethyl)phenyl)boronic acidHCID 8965635965.7%

反応条件

温度45 °C

反応手順

To a suspension of magnesium (0.083 g, 3.42 mmol) in tetrahydrofuran (1.000 mL) was added 0.5 mL of a solution of example 34a (1.099 g, 3.11 mmol) in tetrahydrofuran (1.5 mL). The reaction mixture was warmed (about 40-50° C.) until reaction commenced. The remaining solution of starting bromide was added dropwise. The reaction mixture was stirred at ambient temperature for 1 hour. The resulting Grignard solution was added dropwise to a solution of trimethyl borate (0.696 mL, 6.23 mmol) in tetrahydrofuran (1.5 mL) at 0° C. The reaction mixture was stirred at ambient temperature. After 1 hour at ambient temperature, the reaction mixture was quenched with ice water and then neutralized with 2 M HCl. The mixture was extracted with ethyl acetate (3×). The combined organics were washed with saturated aqueous sodium chloride, dried over anhydrous sodium sulfate, filtered, and concentrated. The crude material was purified by flash chromatography (silica gel, 10-33% ethyl acetate/hexanes) to provide the title compound (0.650 g, 65.7% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09050346B2
出典データセットuspto-grants-2015_06
ORD IDord-80373d6de8154b26ba776e03160b8ebf
出典メモuspto-grants-2015_06