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HRID 476561作成日:2026年10月26日

1-Acetyl-4-(4-nitrophenyl)piperazine → 1-[4-(4-Aminophenyl)piperazin-1-yl]ethan-1-one

https://huagongshe.com/reaction/476561

反応式

関与物質

役割名称HCID仕込み量
反応物1-Acetyl-4-(4-nitrophenyl)piperazineHCID 2865149—
触媒NickelHCID 935—
溶媒EthanolHCID 702—
生成物1-[4-(4-Aminophenyl)piperazin-1-yl]ethan-1-oneHCID 736269—

反応手順

A suspension of 4-acetyl-1-(4-nitrophenyl)piperazine [C. A., 67, P101031Z] (30 g, 0.12 mole) and Raney nickel (2.5 g) in ethanol (500 ml) was hydrogenated at 60 psi (414 kPa) and 40° for 6 hours followed by 18 hours at room temperature. The catalyst was subsequently removed by filtration, the solvent removed under reduced pressure and the residue crystallized from ethyl acetate to yield the title compound, m.p. 129°-130° (18.4 g, 71%), which was used directly in the next stage.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04885294
出典データセットuspto-grants-1989_12
ORD IDord-48c587c122724d43b4582d3b03fd9db0
出典メモuspto-grants-1989_12