HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl iodide → 1-Phenyl-2-benzyl-3,4-dihydroisoquinolinium iodide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl iodide | HCID 12098 | — |
| Reactant | 1-Phenyl-3,4-dihydroisoquinoline | HCID 609926 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1-Phenyl-2-benzyl-3,4-dihydroisoquinolinium iodide | HCID 14721020 | 74.1% |
Reaction Steps
A mixture of 1-phenyl-3,4-dihydroisoquinoline (1.0 g) and benzyliodide (1.26 g) in acetonitrile (7 ml) was refluxed for 1 hour. After allowing to cool to room temperature, the reaction mixture was evaporated in vacuo and the residual precipitate was recrystallized from a mixture of diethyl ether (5 ml) and acetonitrile (3 ml). The crystal was collected by filtration, washed with diethyl ether and dried in vacuo to give 1-phenyl-2-benzyl-3,4-dihydroisoquinolinium iodide (1.52 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05059608 |
| Source dataset | uspto-grants-1991_10 |
| ORD ID | ord-e3457a9e9bca4fb58566c9333f5be9a0 |
| Source note | uspto-grants-1991_10 |