HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cycloheptylamine → N-Cycloheptyl-[(2-phenanthrenyl)methyl]amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cycloheptylamine | HCID 2899 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Methylphenanthrene | HCID 17321 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-Cycloheptyl-[(2-phenanthrenyl)methyl]amine | HCID 15284290 | 66.9% |
Reaction Steps
2-Methylphenanthrene (2.00 g, 10.4 mmol) was brominated with N-bromosuccinimide (2.05 g, 11.5 mmol) and the product compound was added gradually to a suspension of cycloheptylamine (2.38 g, 21.0 mmol) and potassium carbonate (2.90 g, 21.0 mmol) in dimethylformamide (20 ml) with ice-cooling. The mixture was then stirred at room temperature for 16 hrs and, then, filtered and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography to give 2.11 g of a viscous liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05258405 |
| Source dataset | uspto-grants-1993_11 |
| ORD ID | ord-450d9398ff814e4c9fe9af5967e21e18 |
| Source note | uspto-grants-1993_11 |