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HRID 565831作成日:2026年10月25日

1-(4-Nitrobenzyl)piperidine → 4-(Piperidin-1-ylmethyl)aniline

https://huagongshe.com/reaction/565831

反応式

関与物質

役割名称HCID仕込み量
反応物1-(4-Nitrobenzyl)piperidineHCID 783541—
触媒PalladiumHCID 23938—
溶媒EthanolHCID 702—
生成物4-(Piperidin-1-ylmethyl)anilineHCID 84615018.2%

反応手順

In ethanol (50 ml) was dissolved 1-(4-nitrobenzyl)piperidine (6.41 g), and 10% dried palladium on carbon (0.33 g) was added to the mixture. Under hydrogen atmosphere, the mixture was stirred at room temperature under atmospheric pressure for 24 hours. The palladium was filtered off, and the filtrate was concentrated. The residue was recrystallized from hexane to give 1-(4-aminobenzyl)piperidine (1.01 g) as pale yellow crystals.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06172061B2
出典データセットuspto-grants-2001_01
ORD IDord-503b4ff6a8fa4e7798c018ced35f5f00
出典メモuspto-grants-2001_01