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1,4-Dioxane → 2-(2-Fluoro-5-nitrophenyl)pyridine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 1,4-Dioxane | HCID 31275 | — |
| 反応物 | 2-Bromo-1-fluoro-4-nitrobenzene | HCID 69699 | — |
| 反応物 | Sodium Bicarbonate | HCID 516892 | — |
| 生成物 | 2-(2-Fluoro-5-nitrophenyl)pyridine | HCID 22285300 | — |
反応手順
0.55 g of Tetrakis-triphenylphosphine palladium was added to a 1,4-dioxane (20 ml) solution of 2.1 g of 3-bromo-4-fluoro-nitrobenzene and 2.3 g of 2-trimethyltin-pyridine, and the reaction liquid was heated overnight under reflux. Aqueous saturated sodium bicarbonate was added to the reaction liquid, and extracted with ethyl acetate. The organic layer was washed with water and saturated saline, and dried with anhydrous sodium sulfate. The solvent was evaporated away under reduced pressure, and the resulting residue was purified through silica gel column chromatography (developing solvent: hexane/ethyl acetate=7/1) to obtain the entitled compound as a yellow solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07728025B2 |
| 出典データセット | uspto-grants-2010_06 |
| ORD ID | ord-b06ca7ffde7348cc9499a39a52f86f8f |
| 出典メモ | uspto-grants-2010_06 |