HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 67369877, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 67367547 | HCID 67367547 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 67369877 | HCID 67369877 | — |
Reaction Steps
0.65 g (17.1 mmol) of NaBH4 were added in portions to a solution of 3.2 g (max. 14.2 mmol) of the crude product 7-fluoro-1-phenyl-3,4-dihydroisoquinoline in EtOH (80 ml) and the mixture was then stirred for 16 h at RT. Then the mixture was concentrated to small volume under vacuum and the residue was taken up with DCM (200 ml). It was washed with water and the aqueous phase was extracted with DCM (2×150 ml). The combined organic phases were washed with brine, dried over Na2SO4, filtered and concentrated to small volume under vacuum. 7-Fluoro-1-phenyl-1,2,3,4-tetrahydroisoquinoline was obtained as the crude product, which was reacted further with no additional purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08367700B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-4138668e6cef4e1d9b10c6c7ce60c519 |
| Source note | uspto-grants-2013_02 |