Réaction #2315549
ord-d0a27f17fca4480caf5f5daaf7dce84c
Équation de réaction
Réactifs
Aucun
Solvants
Conditions de réaction
Conditions détaillées
See reaction.notes.procedure_details.
Traitement
- 1AutreThe organic layer was separated
- 2Lavagewashed with 100 g of water
- 3Autreevaporated in vacuum
- 4AutreThe residue, 27 g, was purified by silica gel column chromatography (eluent, dichloromethane/methanol)
Mode opératoire
The 4-phenylmethylbenzenesulfonic acid crude product obtained in Synthesis Example 1 was added to the aqueous triphenylsulfonium chloride solution obtained in Synthesis Example 2 and 90 g of dichloromethane, which was stirred for one hour at room temperature. The organic layer was separated, washed with 100 g of water, and evaporated in vacuum. The residue, 27 g, was purified by silica gel column chromatography (eluent, dichloromethane/methanol), obtaining the end product, triphenylsulfonium 4-phenylmethylbenzenesulfonate. It was 21 g (yield 52%) of an oily matter containing a minor amount of solvents (methanol, etc.).