Réaction #155393
ord-883438eaf170468d9b832713eadcafcc
Équation de réaction
Réactifs
Réactifs
Solvants
Conditions de réaction
Traitement
- 1AutreInto a 50 mL round bottom flask equipped with magnetic stirrer
- 2Températurereflux condensor
- 3Températureheating mantle under an argon atmosphere
- 4TempératureThe reaction mixture was refluxed for 2 hrs
- 5Filtrationfiltered
- 6LavageThe solid was washed with 2×25 mL of ethanol
- 7ConcentrationThe combined filtrate was concentrated under reduced pressure
- 8Autreto give off-white solid
- 9Lavagewashed with 100 mL of deionized water
- 10AutreAfter separation the organic layer
- 11Séchagewas dried over anhydrous Na2SO4
- 12Filtrationfiltered
- 13ConcentrationThe solution was concentrated under reduced pressure
- 14Autrepurified by column chromatography on silica gel with 10% ethyl acetate-hexane
Mode opératoire
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-carboxylate. The structure was confirmed as: