HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine,1-(4-nitrophenyl)-4-(4-pyridinyl)- → 1-(4-Aminophenyl)-4-(4-pyridyl)piperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine,1-(4-nitrophenyl)-4-(4-pyridinyl)- | HCID 10924082 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-(4-Aminophenyl)-4-(4-pyridyl)piperazine | HCID 10890461 | 58.3% |
Reaction Steps
A mixture of 1-(4-nitrophenyl)-4-(4-pyridyl)piperazine (2.07 g) in ethanol (100 ml) was hydrogenated at room temperature under a pressure of 2 bars in the presence of 10% palladium on charcoal (0.25 g). When reduction was complete, the catalyst was filtered off and the filtrate was evaporated. The residue was crystallised from methanol/ethyl acetate to give 1-(4-aminophenyl)-4-(4-pyridyl)piperazine (1.08 g), m.p. 210°-211° C. Found: C,70.47; H,7.07; N,21.56. C15H18N4 requires: C,70.83; H,7.13; N,22.03%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04788196 |
| Source dataset | uspto-grants-1988_11 |
| ORD ID | ord-724f0bbbf4eb4edaa1696d9bcefb874d |
| Source note | uspto-grants-1988_11 |