関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 1-Bromo-4-nitrobenzene | HCID 11466 | — |
| 反応物 | 1-Benzylpiperazine | HCID 75994 | — |
| 溶媒 | Water methylene chloride | HCID 21908982 | — |
| 生成物 | 1-Benzyl-4-(4-nitrophenyl)piperazine | HCID 2747427 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08759517B2 |
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| 出典データセット | uspto-grants-2014_06 |
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| ORD ID | ord-58bd338a40824640897be00271babb1d |
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| 出典メモ | uspto-grants-2014_06 |
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