HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → Piperazine, 1-(7-benzofuranyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Tert-butyl 4-(7-benzo[b]furanyl)piperazine-1-carboxylate | HCID 23300012 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Piperazine, 1-(7-benzofuranyl)- | HCID 10465458 | 91.9% |
Reaction Steps
Trifluoroacetic acid (5 ml) was added dropwise at 20° C. under nitrogen to a cooled solution of tert-butyl 4-(7-benzo[b]furanyl)piperazine-1-carboxylate (1.66 g) in dichloromethane (5 ml). The solution was stirred at ambient temperature for 1 hour, then poured into cold water (50 ml). The mixture was basified by the addition of aqueous ammonia solution, then the product was extracted into dichloromethane (2×50 ml). The combined organic extracts were washed with brine (100 ml), dried (MgSO4), and the solvent removed in vacuo to give 1-(7-benzo[b]furanyl)piperazine (1.02 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06114334 |
| Source dataset | uspto-grants-2000_09 |
| ORD ID | ord-1a53f00f6ab24b268f894a684125ceac |
| Source note | uspto-grants-2000_09 |