Reaktion #47818
ord-da7fdcea465a4d1482f088d4455d5142
Reaktionsgleichung
Edukte
Reagenzien
Keine
Lösungsmittel
Reaktionsbedingungen
Temperatur
0°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.
Aufarbeitung
- 1SonstigeUpon the completion of the reaction
- 2Waschenthe mixture washed with saturated saline
- 3Extraktionextracted with ethyl acetate
- 4SonstigeThe organic layer was separated
- 5Trocknendried over anhydrous MgSO4
- 6Einengenconcentrated under a reduced pressure
- 7SonstigeThe resulting residue was purified by flash chromatography
Vorschrift
1-Oxo-3-phenyl-6-(3-phenylpropoxy)-1H-indene-2-carbonitrile (350 mg, 0.878 mmol) obtained in Step 1 was dissolved in THF, and phenylmagnesium chloride (0.483 mL, 0.966 mmol) was added thereto, followed by stirring for 3 hrs at 0° C. Upon the completion of the reaction, the mixture washed with saturated saline and extracted with ethyl acetate. The organic layer was separated, dried over anhydrous MgSO4 and concentrated under a reduced pressure. The resulting residue was purified by flash chromatography to obtain 378 mg of the titled compound (yield: 90%).