HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → Piperazine,1-(4-nitrophenyl)-4-(4-pyridinyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | p-Fluoronitrobenzene | HCID 9590 | — |
| Reactant | 1-(4-Pyridyl)piperazine | HCID 70517 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Water | HCID 962 | — |
| Product | Piperazine,1-(4-nitrophenyl)-4-(4-pyridinyl)- | HCID 10924082 | 51.7% |
Reaction Steps
A mixture of 4-fluoronitrobenzene (7.05 g), 4-pyridylpiperazine (8.15 g), anhydrous sodium bicarbonate (10.0 g) and dry N,N-dimethylformamide (100 ml) was heated under reflux with stirring for 3 hours and then cooled and poured into water. The solid was filtered off, washed with water and crystallised from ethanol to give 1-(4-nitrophenyl)-4-(4-pyridyl)piperazine (7.34 g), m.p. 213°-216° C. Further recrystallisation raised the m.p. to 219°-221° C. Found: C,63.76; H,5.85; N,19.96. C15H16N4O2 requires: C,63.36; H,5.67; N,19.71%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04788196 |
| Source dataset | uspto-grants-1988_11 |
| ORD ID | ord-77428d48f0b845c69e849dca39f58cc8 |
| Source note | uspto-grants-1988_11 |