참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Bromide ion | HCID 259 | — |
| 반응물 | Trimethyl borate | HCID 8470 | — |
| 반응물 | Magnesium | HCID 5462224 | — |
| 반응물 | 2-Bromo-1-(2,4-difluorophenoxy)-4-(trifluoromethyl)benzene | HCID 89656289 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | (2-(2,4-Difluorophenoxy)-5-(trifluoromethyl)phenyl)boronic acid | HCID 89656359 | 66% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09296741B2 |
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| 출처 데이터셋 | uspto-grants-2016_03 |
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| ORD ID | ord-479f508006ca498aad2aa7f9611fdad8 |
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| 출처 메모 | uspto-grants-2016_03 |
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