HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 6-Fluoro-1,2,3,4-tetrahydronaphthalen-2-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 6-Fluoro-1,2,3,4-tetrahydronaphthalen-2-one | HCID 5044385 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 6-Fluoro-1,2,3,4-tetrahydronaphthalen-2-ol | HCID 19699488 | 80% |
Reaction Steps
Sodium borohydride (1.67 g) was added in portions to a solution of 6-fluoro-2-tetralone (6.56 g) in dry ethanol (30 ml) with stirring, keeping the temperature below 25° C. The mixture was then stirred at room temperature for 3 hours. The mixture was then diluted with a little ethyl acetate and concentrated to an oily residue. Dilute sulphuric acid was added dropwise until effervescence no longer occurred. The mixture was extracted with ether and the extract washed, dried, and concentrated to give an oil. This was distilled (b.p. 75-77/0.1 Torr) to give 6-fluorotetralin-2-ol (5.31 g) containing a trace of the tetralone starting material.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04431834 |
| Source dataset | uspto-grants-1984_02 |
| ORD ID | ord-80fcd6266e90474a9d86e62215b9613f |
| Source note | uspto-grants-1984_02 |