HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenethylamine → (2-Phenylethyl)propylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenethylamine | HCID 1001 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Iodopropane | HCID 33643 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (2-Phenylethyl)propylamine | HCID 3142088 | — |
Reaction Steps
1.2 ml (9.5 mmol) of phenylethylamine, 0.93 ml (9.5 mmol) of n-propyl-iodide, 5 ml of triethylamine and 5 ml of THF (tetrahydrofuran) were placed in a flask, and the reaction mixture was heated at reflux temperature of the reaction mixture for 3.5 hours and then cooled. A salt formed was filtered off, the solution was evaporated and a desired compound was purified by column chromatography on silica gel (silica gel 60, mobile phase: CHCl3:CH3OH=10:3). This yields 0.62 g (40%) of N-propyl-(β-phenylethyl)amine in the form of the oil (molecular weight: 163.264, formula: C11H17N).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07560474B2 |
| Source dataset | uspto-grants-2009_07 |
| ORD ID | ord-782d417f33de43f2bb4ffa61161c59ce |
| Source note | uspto-grants-2009_07 |