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HRID 930911作成日:2026年10月27日

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

https://huagongshe.com/reaction/930911

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 8965635966%

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 (1.00 mL) was added 0.5 mL of a solution of Example 275a (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 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 for 1 hour, quenched with ice water and then neutralized with 2 M HCl. The mixture was extracted with ethyl acetate. The combined organics were washed with saturated aqueous sodium chloride, dried over anhydrous sodium sulfate, filtered, and concentrated. The residue was purified by flash chromatography (silica gel, 10-33% ethyl acetate/hexanes gradient) to provide the title compound (650 mg, 66% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09296741B2
出典データセットuspto-grants-2016_03
ORD IDord-479f508006ca498aad2aa7f9611fdad8
出典メモuspto-grants-2016_03