HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 409672Generated: October 26, 2026
1-Bromo-4-nitrobenzene → 1-Benzyl-4-(4-nitrophenyl)piperazine
https://huagongshe.com/reaction/409672
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Bromo-4-nitrobenzene | HCID 11466 | — |
| Reactant | 1-Benzylpiperazine | HCID 75994 | — |
| Solvent | Water methylene chloride | HCID 21908982 | — |
| Product | 1-Benzyl-4-(4-nitrophenyl)piperazine | HCID 2747427 | — |
Reaction Steps
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).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08759517B2 |
|---|
| Source dataset | uspto-grants-2014_06 |
|---|
| ORD ID | ord-58bd338a40824640897be00271babb1d |
|---|
| Source note | uspto-grants-2014_06 |
|---|