Реакция #155393

ord-883438eaf170468d9b832713eadcafcc

Уравнение реакции

C[n+]1c2ccccc2c(C(=O)Oc2ccc(O[Si](C)(C)C(C)(C)C)cc2)c2ccccc21.O=S(=O)([O-])C(F)(F)F
4-(tert-butyldimethylsilyloxy)phenyl 10-methylacridinium-9-carboxylate trifluoromethanesulfonate
[Cl-].[NH4+]
NH4Cl
CN1c2ccccc2C(C(=O)Oc2ccc(O)cc2)c2ccccc21
4-Hydroxyphenyl 10-methylacridan-9-carboxylate

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеInto a 50 mL round bottom flask equipped with magnetic stirrer
  2. 2
    Температураreflux condensor
  3. 3
    Температураheating mantle under an argon atmosphere
  4. 4
    ТемператураThe reaction mixture was refluxed for 2 hrs
  5. 5
    Фильтрацияfiltered
  6. 6
    ПромывкаThe solid was washed with 2×25 mL of ethanol
  7. 7
    КонцентрированиеThe combined filtrate was concentrated under reduced pressure
  8. 8
    Другоеto give off-white solid
  9. 9
    Промывкаwashed with 100 mL of deionized water
  10. 10
    ДругоеAfter separation the organic layer
  11. 11
    Сушкаwas dried over anhydrous Na2SO4
  12. 12
    Фильтрацияfiltered
  13. 13
    КонцентрированиеThe solution was concentrated under reduced pressure
  14. 14
    Другоеpurified 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-carboxylate. The structure was confirmed as:

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08822233B2uspto-grants-2014_09