HuagongsheHuagongshe Chemistry Print Report · For research reference only
Azepane → 1-[(3-Nitrophenyl)methyl]azepane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Azepane | HCID 8119 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Benzene, 1-(bromomethyl)-3-nitro- | HCID 77568 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-[(3-Nitrophenyl)methyl]azepane | HCID 763978 | 70.1% |
Reaction Steps
To a solution of 3-nitrobenzyl bromide (10.5 g, 48.7 mmol) in methylene chloride is added azepane (5.5 mL, 48.7 mmol) and 20.0 mL (146.1 mmol) of triethylamine, and the reaction solution is heated at 60□C under N2 for 20 minutes. After evaporating to dryness, the resulting brown residue is dissolved in methylene chloride and washed twice with saturated Na2CO3 solution, and once with brine solution. After drying over Mg2SO4, the organic solution is filtered and concentrated to give 8.0 g (70.1% yield) of brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07713994B2 |
| Source dataset | uspto-grants-2010_05 |
| ORD ID | ord-899373b4ba1c42f09bfccab3bb9a0aa6 |
| Source note | uspto-grants-2010_05 |