HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Indanone, 3-phenyl- → 1-Phenyl-1H-indene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Indanone, 3-phenyl- | HCID 98146 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Phenyl-1H-indene | HCID 519674 | 50% |
Reaction Steps
Keeping the temperature at -5° C., to a suspension of 5.0 g (0.131 moles) of LiAlH4 in 300 ml of ethyl ether, 35 g (0.168 moles) is added of 3-phenyl-1-indanone dissolved in 50 ml of THF. The oil obtained by evaporating ether (40 g), is dissolved in 300 ml of toluene containing 20 g of Sio2 and kept refluxing for 2 hours, with formed water being distilled off. The resulting mixture is filtered, the solvent is evaporated and by distillation 18 g is obtained (yield of 50%) of 1-phenylindene boiling at 95-100° C./0.2 mm Hg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06124413 |
| Source dataset | uspto-grants-2000_09 |
| ORD ID | ord-8a0a0677b4274248aa2ebcbb3444a03c |
| Source note | uspto-grants-2000_09 |