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Potassium Carbonate → 1-(2',5',5-Trifluoro-1,1'-biphenyl-2-yl)ethanone
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | (2,5-Difluorophenyl)boronic acid | HCID 2734335 | — |
| 反応物 | 1-(2-Bromo-4-fluorophenyl)ethan-1-one | HCID 2736304 | — |
| 触媒 | Tetrabutylammonium Bromide | HCID 74236 | — |
| 触媒 | palladium(II) acetate | HCID 167845 | — |
| 生成物 | 1-(2',5',5-Trifluoro-1,1'-biphenyl-2-yl)ethanone | HCID 22482274 | 27.2% |
反応手順
The title compound was prepared from 2,5-difluorophenylboronic acid (2.0 g, 12.7 mmol), tetrabutylammonium bromide (3.71 g, 11.5 mmol), potassium carbonate (4.78 g, 34.6 mmol), 2′-bromo-4′-fluoroacetophenone (2.5 g, 11.5 mmol), and palladium acetate (259 mg, 1.15 mmol) according to the procedure and in the same manner as described in Example 105, step a. The product was purified by preparative liquid chromatography on a Biotage® 40 Mi column of prepacked silica gel (90 g), eluting with a gradient of 10%-30% methyl tert-butyl ether in hexane, to afford the desired compound (784 mg, 27%) as a clear yellow oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06894061B2 |
| 出典データセット | uspto-grants-2005_05 |
| ORD ID | ord-2d0eb55734bf4c42a36d138b27b01c32 |
| 出典メモ | uspto-grants-2005_05 |