Reaktion #1781818

ord-79e3a3481ac24f83b6ebdc15b9ce8445

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 a 1N sodium hydroxide aqueous solution
  2. 2
    SonstigeThen, the product was purified by silica gel column chromatography (eluent; hexane:ethyl acetate=4:1)

Vorschrift

To an acetonitrile solution (20 ml) of 4-aminothiophenol (1.25 g, 9.98 mmol) and triethylamine (1.11 g, 11.0 mmol) was added 1-iodoheptafluoro-n-propane (5.91 g, 19.9 mmol), and the resultant mixture was stirred at room temperature for 3 hours. The mixture was diluted with ether, and washed with a 1N sodium hydroxide aqueous solution. Then, the product was purified by silica gel column chromatography (eluent; hexane:ethyl acetate=4:1) to obtain 1.85 g (yield 63%) of the title compound.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08158814B2uspto-grants-2012_04