HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 1-(4-Trifluoromethoxyphenyl)-1,2,3,4-tetrahydro-isoquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 1-(4-Trifluoromethoxyphenyl)-3,4-dihydro-isoquinoline | HCID 21264376 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-(4-Trifluoromethoxyphenyl)-1,2,3,4-tetrahydro-isoquinoline | HCID 21264406 | — |
Reaction Steps
The above 1-(4-trifluoromethoxyphenyl)-3,4-dihydro-isoquinoline (0.40 g, 1.4 mmol) was dissolved in methanol (20 mL) and sodium borohydride (0.08 g, 2.1 mmol) was added slowly. The reaction mixture was stirred at room temperature for 2.5 hours. The mixture was evaporated in vacuo, redissolved in 1 N NaOH (20 mL) and extracted with dichloromethane (50 mL). The organic phase was dried (MgSO4), filtered and evaporated in vacuo. The remaining oil (0.35 g) was purified by column chromatography on silica gel eluting with a mixture of dichloromethane and methanol (9:1). This afforded 0.56 g (56%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06177443B1 |
| Source dataset | uspto-grants-2001_01 |
| ORD ID | ord-3315afc3abdf4e7aac800e6cc6432e12 |
| Source note | uspto-grants-2001_01 |