Reaktion #58882

ord-a9064075b6f744c19024d33c4e103b56

Reaktionsgleichung

O
water
Nc1cccc(C#Cc2ccc(OC(F)F)cc2)c1
3-{[4-(difluoromethoxy)phenyl]ethynyl}aniline
c1ccncc1
pyridine
CCS(=O)(=O)Cl
ethylsulfonyl chloride
CCS(=O)(=O)Nc1cccc(C#Cc2ccc(OC(F)F)cc2)c1
N-(3-{[4-(difluoromethoxy)phenyl]ethynyl}phenyl)ethanesulfonamide
Ausbeute 91.4%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Extraktionextracted with EtOAc/ethyl ether 1/1
  2. 2
    Trocknendried over MgSO4
  3. 3
    Einengenconcentrated in vacuo
  4. 4
    SonstigePurification of the resultant residue on silica gel (Biotage)

Vorschrift

A cold (0° C.) solution of 3-{[4-(difluoromethoxy)phenyl]ethynyl}aniline (0.5 g, 1.93 mmol) and pyridine (0.31 mL, 3.80 mmol) in CH2Cl2 was treated dropwise with ethylsulfonyl chloride (0.27 mL, 2.89 mmol). The mixture was stirred for 5 hours, poured into water and extracted with EtOAc/ethyl ether 1/1. The organic extracts were combined, dried over MgSO4 and concentrated in vacuo. Purification of the resultant residue on silica gel (Biotage) using hexanes/EtOAc (3/1) as the eluting solvent gave N-(3-{[4-(difluoromethoxy)phenyl]ethynyl}phenyl)ethanesulfonamide as a yellow oil (0.62 g).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07423158B2uspto-grants-2008_09