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Triethylamine → 4-[(5-Nitro-furan-2-yl)-ethynyl]benzonitrile
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | 2-Bromo-5-nitrofuran | HCID 233582 | — |
| 反応物 | 4-Ethynylbenzonitrile | HCID 4547245 | — |
| 触媒 | HCID 178418476 | HCID 178418476 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | 4-[(5-Nitro-furan-2-yl)-ethynyl]benzonitrile | HCID 19691951 | — |
反応手順
To a solution of 2-bromo-5-nitrofuran (1.65 g) and triethylamine (34 ml) in anhydrous acetonitrile (55 ml) under nitrogen was added bis(triphenylphosphine)palladium dichloride (130 mg) and cuprous iodide (35 mg). 4-Ethynylbenzonitrile (1.09 g) was added and the reaction mixture was stirred under nitrogen overnight. The mixture was evaporated to dryness and the residue was dissolved in dichloromethane (200 ml), dried over anhydrous sodium sulfate, filtered and evaporated to dryness. The residue was purified by silica gel chromatography (ethyl acetate/hexane 1:10) and triturated with ethyl acetate/hexane (1:3) to give 4-[(5-nitro-2-furyl)-ethynyl]benzonitrile.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05726195 |
| 出典データセット | uspto-grants-1998_03 |
| ORD ID | ord-fd2ce529eb5e4230a968d9b7a9207cfc |
| 出典メモ | uspto-grants-1998_03 |