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HRID 1975061作成日:2026年10月26日

N-bromobutanimide → 1-(4-Methylphenyl)-4-bromo-2-cyanopyrrole

https://huagongshe.com/reaction/1975061

反応式

関与物質

役割名称HCID仕込み量
反応物N-bromobutanimideHCID 67184—
反応物1-(4-Methylphenyl)pyrrole-2-carbonitrileHCID 2797715—
溶媒TetrahydrofuranHCID 8028—
生成物1-(4-Methylphenyl)-4-bromo-2-cyanopyrroleHCID 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

DOI10.6084/m9.figshare.5104873.v1
特許番号US05284841
出典データセットuspto-grants-1994_02
ORD IDord-38b6c2f917fe4be0bf1aef398b654f2b
出典メモuspto-grants-1994_02