HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine → (2-Fluoro-phenyl)-piperazin-1-yl-methanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-fluoro-N-phenylbenzenecarbohydrazonoyl chloride | HCID 72745343 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | Phenylhydrazine | HCID 7516 | — |
| Product | (2-Fluoro-phenyl)-piperazin-1-yl-methanone | HCID 544862 | 55.8% |
Reaction Steps
To a stirred mixture of 12.5 parts of piperazine, 3.6 parts of N,N-diethylethanamine and 75 parts of trichloromethane was added a solution of 9 parts of 2-fluoro-N-phenyl-benzenecarbohydrazonoyl chloride in 75 parts of trichloromethane. The whole was stirred for 2 hours at room temperature. After the addition of 5 parts of potassium carbonate, the reaction mixture was stirred for 30 minutes at reflux temperature. The mixture was cooled, washed with 100 parts of water and the layers were separated. The organic layer was dried, filtered and evaporated, yielding 6 parts (55.8%) of 1-(2-fluorobenzoyl)-piperazine, 2-phenylhydrazine as a residue (int. 9).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04957916 |
| Source dataset | uspto-grants-1990_09 |
| ORD ID | ord-dd565b7f8f08445dba38c93306b8a538 |
| Source note | uspto-grants-1990_09 |