HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 2-[N-Benzyl-N-(3,3-diphenylpropyl)amino]methyl-6-methoxytetralin
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3,3-Diphenylpropyl iodide | HCID 15512878 | — |
| Reactant | 2-(N-benzylamino)methyl-6-methoxytetralin hydrochloride | HCID 22998625 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-[N-Benzyl-N-(3,3-diphenylpropyl)amino]methyl-6-methoxytetralin | HCID 18361581 | 37.2% |
Reaction Steps
2-(N-benzylamino)methyl-6-methoxytetralin hydrochloride (0.602 g; obtained in Reference Example 6), 3,3-diphenylpropyl iodide (0.803 g) and potassium carbonate (0.800 g) were added to DMF (20 ml). The reaction mixture was stirred at room temperature for 24 hours, and water was added thereto, which was then extracted with ethyl acetate. The organic layer was washed with water and a saturated aqueous sodium chloride solution, then dried, and concentrated. The residue was purified by silica gel column chromatography (eluent: ethyl acetate/hexane=1/1) to obtain the entitled compound (0.335 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06310107B1 |
| Source dataset | uspto-grants-2001_10 |
| ORD ID | ord-742c9a88866d4323b2ef711663575cc9 |
| Source note | uspto-grants-2001_10 |