Réaction #2315549

ord-d0a27f17fca4480caf5f5daaf7dce84c

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    AutreThe organic layer was separated
  2. 2
    Lavagewashed with 100 g of water
  3. 3
    Autreevaporated in vacuum
  4. 4
    AutreThe 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.).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US06416928B1uspto-grants-2002_07