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Borane;tetrahydrofuran → 2-Bromo-5-(trifluoromethyl)benzyl alcohol
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Borane;tetrahydrofuran | HCID 2723981 | — |
| 反応物 | 2-Bromo-5-(trifluoromethyl)benzoic acid | HCID 15261013 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 2-Bromo-5-(trifluoromethyl)benzyl alcohol | HCID 2756248 | 100.1% |
反応手順
To an ice-cooled solution of 2-bromo-5-(trifluoromethyl)benzoic acid (5.16 g, 19 mmol) in THF (50 mL) was added borane-tetrahydrofuran complex (70 mL of 1M solution in THF, 70 mmol). The resulting mixture was stirred at room temperature for 16 hours. The reaction mixture was quenched with methanol. Solvent was removed. The residue was partitioned between ethyl acetate (3×40 mL) and 1M sodium bicarbonate (50 mL). The combined organic layers were washed with saturated NaCl (50 mL), dried (MgSO4) and concentrated to yield the title compound as an oil (4.85 g). 1H NMR (400 MHz, CDCl3) δ 4.8 (s, 2 H) 7.5 (m, 1 H) 7.7 (d, J=8.2 Hz, 1 H) 7.8 (d, J=1.6 Hz, 1 H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08383660B2 |
| 出典データセット | uspto-grants-2013_02 |
| ORD ID | ord-0ba15b80095a49f089ecf99eacfd814e |
| 出典メモ | uspto-grants-2013_02 |