HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Bromo-1-indanone → 5-bromo-2,3-dihydro-1H-inden-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Bromo-1-indanone | HCID 520695 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-bromo-2,3-dihydro-1H-inden-1-ol | HCID 13486299 | 98.8% |
Reaction Steps
To a solution of 5-bromo-1-indanone (2.0 g, 9.5 mmol) in THF (20 mL) was added NaBH4 (0.5 g, 12.8 mmol). After stirring at room temperature overnight, the solution was quenched by addition of water. The resulting solution was extracted with EtOAc twice. The combined EtOAc layers were dried over Na2SO4 and concentrated under vacuum to give 2.0 g of the title compound as a solid. MS calculated for C9H9BrO: (M+H)+212.9; found 194.9 (M+H—H2O)+, 197.0 (M+H—H2O)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09067921B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-c8cb10f4432a420a8176ebc758bc9dea |
| Source note | uspto-grants-2015_06 |