HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hexahydro-1,4-diazepine → 1-(2-Fluoro-4-nitrophenyl)homopiperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hexahydro-1,4-diazepine | HCID 68163 | — |
| Reactant | 1,2-Difluoro-4-nitrobenzene | HCID 123053 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1-(2-Fluoro-4-nitrophenyl)homopiperazine | HCID 22291169 | 77.3% |
Reaction Steps
To homopiperazine (5 g, 0.05 mol) in acetonitrile (30 mL), 3.4-difluoronitrobenzene (3.17 g, 0.02 mol) was added and the reaction mixture was heated to reflux for 4 hrs. Then the solvent was evaporated and the residue taken in EtOAc and washed with water and brine solution. The EtOAc layer was dried over anhyd Na2SO4 and evaporated in vacuo. The residue was digested with ether-hexane (1:20), decanted and dried in vacuo to get 3.7 g of final product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06734307B2 |
| Source dataset | uspto-grants-2004_05 |
| ORD ID | ord-8c0275b69b064c2fa1c033cbdef0d573 |
| Source note | uspto-grants-2004_05 |