Reaktion #1760747
ord-51665185760c4980a144e588644e73c2
Reaktionsgleichung
Edukte
Lösungsmittel
Reaktionsbedingungen
Aufarbeitung
- 1Temperaturthe resulting mixture was heated
- 2Temperaturto reflux for 2 hours
- 3Temperaturthe resulting mixture was heated
- 4Temperaturto reflux for 6 hours
- 5TemperaturAfter the reaction mixture was cooled to room temperature
- 6SonstigeThe organic layer was separated
- 7Trocknendried over anhydrous magnesium sulfate
- 8Waschenafter washed with a saturated sodium chloride aqueous solution
- 9Sonstigethe solvent was evaporated under reduced pressure
- 10SonstigeThe obtained residue was purified with silica gel column chromatography [PSQ100B (spherical) manufactured by Fuji Silysia Chemical Ltd., eluent; hexane:ethyl acetate=10:1]
Vorschrift
86 mg of 4-phenylpiperidine, 0.22 g of cesium carbonate, 2.4 mg of tris(dibenzylideneacetone)dipalladium(0), 1.2 mg of palladium acetate and 6.3 mg of 2-dicyclohexylphosphino-2′,4′,6′-triisopropylbiphenyl were added to 3.0 mL of toluene solution containing 0.10 g of tert-butyl 2-(benzamido)-4-bromobenzoate, and the resulting mixture was heated to reflux for 2 hours. After the reaction mixture was cooled to room temperature, 2.4 mg of tris(dibenzylideneacetone)dipalladium(0), 1.2 mg of palladium acetate and 6.3 mg of 2-dicyclohexylphosphino-2′,4′,6′-triisopropylbiphenyl were added and the resulting mixture was heated to reflux for 6 hours. After the reaction mixture was cooled to room temperature, ethyl acetate and 10% citric acid aqueous solution were added. The organic layer was separated and dried over anhydrous magnesium sulfate after washed with a saturated sodium chloride aqueous solution, and the solvent was evaporated under reduced pressure. The obtained residue was purified with silica gel column chromatography [PSQ100B (spherical) manufactured by Fuji Silysia Chemical Ltd., eluent; hexane:ethyl acetate=10:1] to obtain tert-butyl 2-(benzamido)-4-(4-phenylpiperidin-1-yl)benzoate as pale yellow solid.