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Borohydride → (2-Amino-5-bromo-3-fluorophenyl)methanol
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Borohydride | HCID 28123 | — |
| 反応物 | 2-Amino-5-bromo-3-fluorobenzoic acid | HCID 40424597 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | (2-Amino-5-bromo-3-fluorophenyl)methanol | HCID 54312525 | 95% |
反応手順
To a solution of 2-amino-5-bromo-3-fluorobenzoic acid (14.5 g, 62.2 mmol) in THF (150 mL) at 0° C. was added borohydride in THF (1 M, 310 mL), and the reaction mixture was stirred at room temperature overnight. The reaction was quenched with methanol (150 mL), concentrated in vacuum, diluted with aqueous sodium bicarbonate (400 mL) and extracted with ethyl acetate (200 mL*3). The organic layers were separated, combined, washed with water (200 mL) and brine (200 mL), dried over sodium sulfate, filtered and concentrated to afford the title compound (13.0 g, crude), which was directly used in the next step without the further purification. MS (ES+) C7H7BrFNO requires: 219, 221, found: 220, 222 [M+H]+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US09434700B2 |
| 出典データセット | uspto-grants-2016_09 |
| ORD ID | ord-cbaeea48176b456eaf135dbfa41aeec5 |
| 出典メモ | uspto-grants-2016_09 |