HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 1-Benzyl-4-(4-nitrophenyl)piperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1-Chloro-4-nitrobenzene | HCID 7474 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Benzylpiperazine | HCID 75994 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-Benzyl-4-(4-nitrophenyl)piperazine | HCID 2747427 | 76% |
Reaction Steps
1-Benzylpiperazine (2.8 ml; 16 mmol) and potassium carbonate (2.3 g; 17 mmol) were added to a solution of 1-chloro-4-nitrobenzene (2.0 g; 13 mmol) in dimethylformamide (0.5 ml), and the mixture was stirred for 7 hours in a bath controlled at 100° C. Water was added to the reaction mixture to conduct extraction with chloroform. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate and then concentrated under reduced pressure. The resultant crude oil was purified by column chromatography on silica gel, thereby obtaining 2.9 g (yield: 76%) of 4-(4-benzyl-1-piperazinyl)-1-nitrobenzene as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06448242B1 |
| Source dataset | uspto-grants-2002_09 |
| ORD ID | ord-0bc24bf1b1694fbea14f394802cda1a6 |
| Source note | uspto-grants-2002_09 |