HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Fluoronitrobenzene → 1-(4-Nitrophenyl)-1,4-diazepane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Fluoronitrobenzene | HCID 9590 | — |
| Reactant | Hexahydro-1,4-diazepine | HCID 68163 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(4-Nitrophenyl)-1,4-diazepane | HCID 5055950 | 82.7% |
Reaction Steps
A solution of hexahydro-1H-1,4-diazepine (0.20 mol) and 1-fluoro-4-nitro-benzene (0.10 mol) in DCM (300 ml) was stirred at room temperature for 24 hours under nitrogen atmosphere. Yellow crystals precipitated. The precipitate was collected on filter, washed with ether and dried. The residue (21.1 g, 87%) was taken up in water and treated with a 3 N NaOH solution. This mixture was extracted with DCM (3×500 ml), dried (Na2SO4), filtered, and the solvent was removed under reduced pressure and dried under vacuum at room temperature for 16 hours, yielding 18.3 g of hexahydro-1-(4-nitrophenyl)-1H-1,4-diazepine (interm. 1), melting point 115-116° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08268833B2 |
| Source dataset | uspto-grants-2012_09 |
| ORD ID | ord-5948c0cbfb284823a96dbc5c044d2208 |
| Source note | uspto-grants-2012_09 |