HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine → HCID 12016523, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | HCID 12016522 | HCID 12016522 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Ammonium Hydroxide | HCID 14923 | — |
| Product | HCID 12016523 | HCID 12016523 | 164% |
Reaction Steps
A mixture of Example 1B (10 g, 42 mmol), KI (8.5 g, 51.2 mmol), K2CO3 (8.75 g, 63.3 mmol), and piperazine (10.75 g, 125 mmol) in 2-butanone (500 mL) was refluxed for 48 hours. The reaction mixture was then cooled to room temperature, treated with 1 M sodium thiosulfate (100 mL) and ethyl acetate (500 mL). The layers were separated, and the organic layer was washed with water and brine, dried (MgSO4), filtered, and concentrated. The concentrate was purified by column chromatography on silica gel using 98:2:0.1 to 95:5:0.9 dichloromethane:methanol:concentrated ammonium hydroxide as the eluant to afford 9.931 g (82%) of the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06559140B2 |
| Source dataset | uspto-grants-2003_05 |
| ORD ID | ord-60a7738f4c1b412eaa534dfa47f0013b |
| Source note | uspto-grants-2003_05 |