HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Chloro-4-nitrobenzene → 1-(4-Nitrophenyl)-1,4-diazepane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Chloro-4-nitrobenzene | HCID 7474 | — |
| Reactant | Hexahydro-1,4-diazepine | HCID 68163 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | 1-(4-Nitrophenyl)-1,4-diazepane | HCID 5055950 | 42% |
Reaction Steps
A solution of homopiperazine (11.4 g, 114 mmol) in 1-butanol (40 mL) was added to a refluxing solution of 1-chloro-4-nitrobenzene (6.0 g, 38 mmol) in 1-butanol (40 mL) over 15 minutes. The mixture was maintained at reflux for 24 hours then cooled to room temperature and extracted with 2N hydrochloric acid. The aqueous layer was basified with potassium carbonate and extracted with ethyl acetate. The organic layer was dried over sodium sulfate and concentrated to afford 1-(4-nitro-phenyl)-[1,4]diazepane (3.5 g, 42%) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08524705B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-4c60e14d135f433dad7b2bd9ef175647 |
| Source note | uspto-grants-2013_09 |