HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Bicarbonate → 7-Methoxy-1-methyl-1,2,3,4-tetrahydroisoquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 7-Methoxy-1-methyl-3,4-dihydroisoquinoline | HCID 15061977 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 7-Methoxy-1-methyl-1,2,3,4-tetrahydroisoquinoline | HCID 15940011 | 94.4% |
Reaction Steps
Sodium cyanoborohydride (0.43 g) was added to a solution of 7-methoxy-1-methyl-3,4-dihydro-isoquinoline (2.67 g) in methanol (41 mL). The mixture was stirred at rt for 20 min. Aqueous sodium bicarbonate (saturated, 10 mL) was added to quench the excess hydride reagent. The methanol was evaporated under vacuum and the aqueous solution was diluted with sodium bicarbonate (saturated, 30 mL) and extracted with dichloromethane (2×30 mL). The combined organic layers were dried over sodium sulfate, filtered and evaporated to afford 7-methoxy-1-methyl-1,2,3,4-tetrahydro-isoquinoline (2.55 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07084154B2 |
| Source dataset | uspto-grants-2006_08 |
| ORD ID | ord-ac6e3f79f8e84358b70ca30390b52cd6 |
| Source note | uspto-grants-2006_08 |