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HRID 409672作成日:2026年10月24日

1-Bromo-4-nitrobenzene → 1-Benzyl-4-(4-nitrophenyl)piperazine

https://huagongshe.com/ja/reaction/409672

反応式

関与物質

役割名称HCID仕込み量
反応物1-Bromo-4-nitrobenzeneHCID 11466—
反応物1-BenzylpiperazineHCID 75994—
溶媒Water methylene chlorideHCID 21908982—
生成物1-Benzyl-4-(4-nitrophenyl)piperazineHCID 2747427—

反応条件

温度80 °C

反応手順

A mixture of 1-bromo-4-nitrobenzene (5 g, 24.8 mmol) and 1-benzylpiperazine (8.6 ml, 49.5 mmol, 2 equiv) is heated to 80° C. for 17 h. The reaction mixture is allowed to cool to RT, and is diluted with DCM/H2O. The layers are separated and the aqueous phase is extracted with DCM. The combined organic phase is washed with brine, dried (Na2SO4), filtered and concentrated. Purification of the residue by silica gel column chromatography (Hex/EtOAc, 1:1) affords the title compound as a yellow solid: ESI-MS: 298.3 [MH]+; tR=3.25 min (purity: 100%, system 1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08759517B2
出典データセットuspto-grants-2014_06
ORD IDord-58bd338a40824640897be00271babb1d
出典メモuspto-grants-2014_06