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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 930911생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/930911

반응식

참여 물질

역할이름HCID투입량
반응물Bromide ionHCID 259—
반응물Trimethyl borateHCID 8470—
반응물MagnesiumHCID 5462224—
반응물2-Bromo-1-(2,4-difluorophenoxy)-4-(trifluoromethyl)benzeneHCID 89656289—
용매TetrahydrofuranHCID 8028—
생성물(2-(2,4-Difluorophenoxy)-5-(trifluoromethyl)phenyl)boronic acidHCID 8965635966%

반응 조건

온도45 °C

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09296741B2
출처 데이터셋uspto-grants-2016_03
ORD IDord-479f508006ca498aad2aa7f9611fdad8
출처 메모uspto-grants-2016_03