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N-bromobutanimide → 1-(4-Methylphenyl)-4-bromo-2-cyanopyrrole
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | N-bromobutanimide | HCID 67184 | — |
| 反応物 | 1-(4-Methylphenyl)pyrrole-2-carbonitrile | HCID 2797715 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 1-(4-Methylphenyl)-4-bromo-2-cyanopyrrole | HCID 18956250 | — |
反応手順
To a solution of 1-(4-methylphenyl)-2-cyanopyrrole (1.274 g) in tetrahydrofuran (25 ml) is added N-bromosuccinimide (1.776 g) in several portions at room temperature. After being stirred for 3 hours at ambient temperature, the mixture is concentrated in vacuo. The residue is treated with diethyl ether. The precipitates are removed by filtration and washed with a small amount of diethyl ether. The filtrates are concentrated in vacuo to give an oily residue, which is purified by silicagel column chromatography (elution by 40% methylene chloride in n-hexane) to yield 1-(4-methylphenyl)-4-bromo-2-cyanopyrrole as a solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05284841 |
| 出典データセット | uspto-grants-1994_02 |
| ORD ID | ord-38b6c2f917fe4be0bf1aef398b654f2b |
| 出典メモ | uspto-grants-1994_02 |