Réaction #1340570

Équation de réaction

Bis(4-hydroxyphenyl)phenylsulfonium triflate

potassium nonaflate

→

white solid

Rendement 61.0%

Bis(4-hydroxyphenyl)Phenylsulfonium Nonaflate

Rendement 61.0%

Solvants

water

water

Conditions de réaction

Traitement

1. 1
   Autreformed a cloudy solution
2. 2
   AutreThe formed oil was separated from the aqueous layer
3. 3
   Autreby decanting this layer away
4. 4
   LavageThe residual oil was washed with 2 mL of distilled water
5. 5
   workup.DISSOLUTIONThis residue was dissolved in 4 mL acetone
6. 6
   ExtractionThis mixture was then extracted with 100 mL of methylene chloride
7. 7
   workup.STIRRINGafter stirring overnight
8. 8
   LavageThe methylene chloride layer was washed with water several times
9. 9
   workup.DISSOLUTIONDissolving in a minimum of methylene chloride the residue
10. 10
    Autrewas precipitated with pentane
11. 11
    Autredried under high vacuum

Mode opératoire

Bis(4-hydroxyphenyl)phenylsulfonium triflate (2.5 g, 0.00739 moles; Dainippon Pharmaceuticals) was dissolved in 20 mL of water in a suitable container to which was added potassium nonaflate (3.28 g, 0.00739 mole). To this mixture was added 120 mL of water, which formed a cloudy solution. This solution was stirred overnight at room temperature in a stoppered flask. The formed oil was separated from the aqueous layer by decanting this layer away. The residual oil was washed with 2 mL of distilled water. This residue was dissolved in 4 mL acetone and another 2.6 g of potassium nonaflate and 100 mL of water. This mixture was then extracted with 100 mL of methylene chloride after stirring overnight. The methylene chloride layer was washed with water several times and stripped of solvents. Dissolving in a minimum of methylene chloride the residue was precipitated with pentane and then dried under high vacuum to give 2.68 g of white solid (61% yield) which was pure by 1H and 19F NMR.

Source