Réaction #312587
ord-f9eabe6b564c4287b4b398c47b0987fc
Équation de réaction
Réactifs
Aucun
Solvants
Conditions de réaction
Conditions détaillées
See reaction.notes.procedure_details.
Traitement
- 1Autresynthesized in Synthesis Example 9
- 2AutreThe organic layer was separated
- 3Lavagewashed with 50 g of water three times
- 4ConcentrationThe organic layer was concentrated
- 5workup.ADDITION25 g of diethyl ether was added to the residue for crystallization
- 6FiltrationThe crystals were filtered
- 7Autredried
- 8Autreobtaining the target compound
Mode opératoire
To 50 g of dichloromethane were added an amount (corresponding to 0.011 mole) of the triphenylsulfonium chloride aqueous solution of Synthesis Example 1 and 3.6 g (0.01 mole) of sodium 2-benzoyloxy-1,1,3,3,3-pentafluoro-propane-1-sulfonate synthesized in Synthesis Example 9, followed by stirring. The organic layer was separated and washed with 50 g of water three times. The organic layer was concentrated and 25 g of diethyl ether was added to the residue for crystallization. The crystals were filtered and dried, obtaining the target compound. White crystals, 4.5 g (yield 75%).