Reaktion #1121769
ord-29c83ed2916046638a483784ba98ab81
Reaktionsgleichung
Edukte
Reagenzien
Lösungsmittel
Reaktionsbedingungen
Aufarbeitung
- 1SonstigeInto a 50 mL round bottom flask equipped with magnetic stirrer
- 2Temperaturreflux condensor
- 3Temperaturheating mantle under an argon atmosphere
- 4TemperaturThe reaction mixture was refluxed for 2 hrs
- 5Filtrationfiltered
- 6WaschenThe solid was washed with 2×25 mL of ethanol
- 7EinengenThe combined filtrate was concentrated under reduced pressure
- 8Sonstigeto give off-white solid
- 9Waschenwashed with 100 mL of deionized water
- 10SonstigeAfter separation the organic layer
- 11Trocknenwas dried over anhydrous Na2SO4
- 12Filtrationfiltered
- 13EinengenThe solution was concentrated under reduced pressure
- 14Sonstigepurified by column chromatography on silica gel with 10% ethyl acetate-hexane
Vorschrift
Into a 50 mL round bottom flask equipped with magnetic stirrer, reflux condensor and heating mantle under an argon atmosphere was charged a solution of 1.42 parts of the 4-(tert-butyldimethylsilyloxy)phenyl 10-methylacridinium-9-carboxylate trifluoromethanesulfonate in 200 mL of ethanol. Then 16 arts NH4Cl was added in five portions, followed by 19.3 parts of Zn in five portions to a hot yellow solutions causing immediate decolorization of the solution. The reaction mixture was refluxed for 2 hrs and filtered. The solid was washed with 2×25 mL of ethanol. The combined filtrate was concentrated under reduced pressure to give off-white solid. The solid was dissolved in 250 mL of dichloromethane and washed with 100 mL of deionized water. After separation the organic layer was dried over anhydrous Na2SO4 and filtered. The solution was concentrated under reduced pressure and purified by column chromatography on silica gel with 10% ethyl acetate-hexane to yield 0.76 parts of 4-Hydroxyphenyl 10-methylacridan-9-carboxvlate. The structure was confirmed as: