HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → HCID 12473037, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | 3,4-Dihydro-6,7-dimethoxy-1-methylisoquinoline | HCID 22652 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 12473037 | HCID 12473037 | 81% |
Reaction Steps
To a stirred solution of 1-methyl-6,7-dimethoxy-3,4-dihydroisoquinoline in acetone was added benzyl bromide and the reaction mixture was stirred at room temperature for 16 hours. A yellow precipitate formed which was filtered, washed with ice cold acetone and dried in vacuo. The product was further purified by recrystallisation from a hexane/dichloromethane mix and pentane to afford the desired compound in 81% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06509467B1 |
| Source dataset | uspto-grants-2003_01 |
| ORD ID | ord-c824390635014efbb577f2fb46e1a921 |
| Source note | uspto-grants-2003_01 |