HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → N-Cycloheptyl-[(2-fluorenyl)methyl]amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Cycloheptylamine | HCID 2899 | — |
| Reactant | Fluorene-2-carboxaldehyde | HCID 34804 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-Cycloheptyl-[(2-fluorenyl)methyl]amine | HCID 15284282 | 92.4% |
Reaction Steps
2-Formylfluorene (2.27 g, 11.7 mmol) and cycloheptylamine (1.39 g, 12.3 mmol) were heated together at 120° C. for 14 hrs. After cooling, the reaction mixture was distilled under reduced pressure. Then, ethanol (30 ml) and sodium borohydride (0.44 g, 11.7 mmol) were added to the residue and the mixture was stirred for 0.5 hr. The mixture was then diluted with water (100 ml) and extracted with chloroform (80 ml×2 times). The organic layer was dried over anhydrous magnesiumsulfate. The solvent was then distilled off under reduced pressure to give 3.15 g of a pale yellow solid residue.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05420348 |
| Source dataset | uspto-grants-1995_05 |
| ORD ID | ord-cbaaad8d1e694595b94773f37e5b580e |
| Source note | uspto-grants-1995_05 |