Reaktion #828867

ord-6cee9216ac6e4bdb8514fb3f798c7c14

Reaktionsgleichung

CS(=O)(=O)c1ccc(CC(O)c2ccc(F)cc2)cc1
product
CS(=O)(=O)c1ccc(CC(O)c2ccc(F)cc2)cc1
1-(4-Fluorophenyl)-2-(4-(methylsulfonyl)phenyl)ethanol
[O]=[Cr](=[O])([O-])[Cl].c1cc[nH+]cc1
PCC
CS(=O)(=O)c1ccc(CC(=O)c2ccc(F)cc2)cc1
title compound
Ausbeute 96.2%
CS(=O)(=O)c1ccc(CC(=O)c2ccc(F)cc2)cc1
1-(4-Fluorophenyl)-2-(4-(methylsulfonyl)phenyl)ethanone
Ausbeute 96.2%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Filtrationfiltered through a short pad of silica gel (eluted with acetone)
  2. 2
    EinengenThe eluant was concentrated
  3. 3
    Sonstigethe residue was chromatographed on silica gel (eluted with 30 % EtOAc/CH2Cl2)

Vorschrift

To a cold (0° C.) solution of the product of step 2 (5.45 g, 18.5 mmol) in CH2C2 (350 mL) was added PCC (6.13 g, 28 mmol). The mixture was stirred at r.t. for 6.5 h and filtered through a short pad of silica gel (eluted with acetone). The eluant was concentrated and the residue was chromatographed on silica gel (eluted with 30 % EtOAc/CH2Cl2) to give 5.2 g of the title compound.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05552422uspto-grants-1996_09