Reaktion #2007686

ord-8559646654e64d55a6c5bdc004f06fbc

Reaktionsgleichung

CC#N
acetonitrile
Nc1ccc(S)cc1
4-aminothiophenol
CCN(CC)CC
triethylamine
FC(F)(F)C(F)(F)C(F)(F)I
1-iodoheptafluoro-n-propane
Nc1ccc(SC(F)(F)C(F)(F)C(F)(F)F)cc1
title compound
Ausbeute 63.2%
Nc1ccc(SC(F)(F)C(F)(F)C(F)(F)F)cc1
4-(heptafluoro-n-propylthio)aniline
Ausbeute 63.2%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Waschenwashed with an aqueous solution of 1N sodium hydroxide
  2. 2
    Sonstigepurified by silica gel column chromatography (eluent:hexane:ethyl acetate=4:1)

Vorschrift

To 20 ml of an acetonitrile solution of 1.25 g of 4-aminothiophenol and 1.11 g of triethylamine, 5.91 g of 1-iodoheptafluoro-n-propane was added, and the mixture was stirred at room temperature for 3 hours. The mixture was diluted with ether, washed with an aqueous solution of 1N sodium hydroxide and purified by silica gel column chromatography (eluent:hexane:ethyl acetate=4:1) to give 1.85 g (yield 63%) of the title compound.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08168825B2uspto-grants-2012_05