HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Fluoronitrobenzene → 4-[4-(4-Nitrophenyl)piperazin-1-yl]phenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Fluoronitrobenzene | HCID 9590 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Dimethylacetamide | HCID 31374 | — |
| Reactant | p-(1-Piperazinyl)phenol | HCID 92467 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-[4-(4-Nitrophenyl)piperazin-1-yl]phenol | HCID 11381017 | 76% |
Reaction Steps
A mixture of 91.7 parts of 4-(1-piperazinyl)phenol, 71.0 parts of 1-fluoro-4-nitrobenzene, 60.0 parts of potassium carbonate and 450 parts of N,N-dimethylacetamide was stirred over weekend at room temperature. Water was added and after standing for 5 hours, the product was filtered off. It was purified by column chromatography over silica gel using trichloromethane as eluent. The pure fractions were collected and the eluent was evaporated, yielding 114.4 parts (76%) of 4-[4-(4-nitrophenyl)-1-piperazinyl]phenol; mp. 260.0° C. (intermediate 9).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04791111 |
| Source dataset | uspto-grants-1988_12 |
| ORD ID | ord-65f369ebf2fb4e74a62466c2ab3c178a |
| Source note | uspto-grants-1988_12 |