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HRID 1079392作成日:2026年10月25日

Piperidine → Piperidine, 1-(4-nitrophenyl)-

https://huagongshe.com/reaction/1079392

反応式

関与物質

役割名称HCID仕込み量
反応物PiperidineHCID 8082—
反応物p-FluoronitrobenzeneHCID 9590—
溶媒DimethylformamideHCID 6228—
生成物Piperidine, 1-(4-nitrophenyl)-HCID 81049—

反応手順

A solution of p-fluoronitrobenzene (31.8 ml) in dimethylformamide (200 ml) was ice-cooled and to this was added piperidine (60 ml) dropwise, followed by stirring with ice cooling for 2 hours. After the solvent was distilled off, the residual oily product was dissolved in ethyl acetate ester (200 ml), followed by washing in turn with aqueous saturated solution of sodium bicarbonate and water. Then, the solution was dried over anhydrous magnesium sulfate. After the solvent was distilled off, the residue was recrystallized from n-hexane to obtain N-(4-nitrophenyl)piperidine as yellow crystals (52.8 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05580883
出典データセットuspto-grants-1996_12
ORD IDord-2cf7a327371f4730a5c5bfa29490dc36
出典メモuspto-grants-1996_12