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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 361948Erstellt: 25. Oktober 2026

1-Indanone → 1-Phenyl-1H-indene

https://huagongshe.com/reaction/361948

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-IndanoneHCID 6735—
Edukt1-Phenyl-1-indanolHCID 12254758—
EduktHCID 178418255HCID 178418255—
LösungsmittelDiethyl EtherHCID 3283—
Produkt1-Phenyl-1H-indeneHCID 51967495,9%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05866704
Quelldatensatzuspto-grants-1999_02
ORD IDord-b31589cc69694298b5602cf2d3cb8cc0
Quellennotizuspto-grants-1999_02