関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Bromide ion | HCID 259 | — |
| 反応物 | Trimethyl borate | HCID 8470 | — |
| 反応物 | Magnesium | HCID 5462224 | — |
| 反応物 | 2-Bromo-1-(2,4-difluorophenoxy)-4-(trifluoromethyl)benzene | HCID 89656289 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | (2-(2,4-Difluorophenoxy)-5-(trifluoromethyl)phenyl)boronic acid | HCID 89656359 | 66% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09296741B2 |
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| 出典データセット | uspto-grants-2016_03 |
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| ORD ID | ord-479f508006ca498aad2aa7f9611fdad8 |
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| 出典メモ | uspto-grants-2016_03 |
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