HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → 6-bromo-4,7-difluoro-2,3-dihydro-1H-inden-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 6-bromo-4,7-difluoro-2,3-dihydro-1H-inden-1-one | HCID 86715126 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 6-bromo-4,7-difluoro-2,3-dihydro-1H-inden-1-ol | HCID 86715125 | — |
Reaction Steps
To a mixture of 6-bromo-4,7-difluoro-2,3-dihydro-1H-inden-1-one (0.5 g), THF (1 mL) and EtOH (1 mL) was added NaBH4 (100 mg). After 1 hour the reaction mixture was concentrated and the residue distributed between water and EA. The organic phase was washed with water (3 times), dried (Na2SO4), filtered and concentrated. The residue was purified by preparative HPLC to provide the subtitle compound. MS ESI+: m/z=249 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08853412B2 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-e5ef06cd3da54bd6adf90fe761e47c69 |
| Source note | uspto-grants-2014_10 |