Reaktion #51269

ord-cc4dd4a925134e97806965f18a207e98

Reaktionsgleichung

CC(C)=CCBr
1-bromo-3-methyl-2-butene
Sc1ccccc1Br
2-bromothiophenol
CN(C)C=O
DMF
O=C([O-])[O-].[K+].[K+]
potassium carbonate
CC(C)=CCSc1ccccc1Br
2-bromo-1-(3-methylbut-2-enylthio)benzene

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Extraktionextracted with ethyl acetate
  2. 2
    Sonstigethe organic phase is separated
  3. 3
    Waschenwashed with water
  4. 4
    Trocknendried over magnesium sulphate
  5. 5
    Sonstigeevaporated
  6. 6
    Sonstige26.00 g (99%) of the expected compound are collected in the form of an orangey oil

Vorschrift

19.30 g (102.0 mmol) of 2-bromothiophenol, 160 ml of DMF and 15.50 g (112.0 mmol) of potassium carbonate are introduced into a three-necked flask. 13 ml (112.0 mmol) of 1-bromo-3-methyl-2-butene are added dropwise and the reaction mixture is stirred at room temperature for two hours. It is poured into water and extracted with ethyl acetate and the organic phase is separated by settling, washed with water, dried over magnesium sulphate and evaporated. 26.00 g (99%) of the expected compound are collected in the form of an orangey oil.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06849658B2uspto-grants-2005_02