HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
1-Indanone → 1-Phenyl-1H-indene
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 1-Indanone | HCID 6735 | — |
| Edukt | 1-Phenyl-1-indanol | HCID 12254758 | — |
| Edukt | HCID 178418255 | HCID 178418255 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Produkt | 1-Phenyl-1H-indene | HCID 519674 | 95,9% |
Reaktionsschritte
1-Indanone (13.30 g, 0.1006 moles) was stirred in diethylether (300 mL) at -78° C. as PhMgBr (0.150 moles, 50.00 mL of 3.0M solution in diethylether) was added. The mixture was then allowed to slowly warm to 20°-25° C. and then stirred 16 hours. After the reaction period the mixture was poured on ice and then extracted with aqueous solutions of 1M HCI (1×100 mL), 1M NaHCO3 (1×100 mL), andthen H2O (1×100 mL). The organic layer was then dried over MgSO4. Filtration followed by removal of the volatiles resulted in the isolation of a yellow oil which by NMR was seen to still contain some 1-phenyl-1-indanol. This oil was then distilled under vacuum to yield the desired product as a pale yellow oil (18.56 g, 95.9 percent).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05866704 |
| Quelldatensatz | uspto-grants-1999_02 |
| ORD ID | ord-b31589cc69694298b5602cf2d3cb8cc0 |
| Quellennotiz | uspto-grants-1999_02 |