Реакция #1121769
ord-29c83ed2916046638a483784ba98ab81
Уравнение реакции
Реактанты
Реагенты
Растворители
Условия реакции
Обработка
- 1ДругоеInto a 50 mL round bottom flask equipped with magnetic stirrer
- 2Температураreflux condensor
- 3Температураheating mantle under an argon atmosphere
- 4ТемператураThe reaction mixture was refluxed for 2 hrs
- 5Фильтрацияfiltered
- 6ПромывкаThe solid was washed with 2×25 mL of ethanol
- 7КонцентрированиеThe combined filtrate was concentrated under reduced pressure
- 8Другоеto give off-white solid
- 9Промывкаwashed with 100 mL of deionized water
- 10ДругоеAfter separation the organic layer
- 11Сушкаwas dried over anhydrous Na2SO4
- 12Фильтрацияfiltered
- 13КонцентрированиеThe solution was concentrated under reduced pressure
- 14Другоеpurified by column chromatography on silica gel with 10% ethyl acetate-hexane
Методика
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: