Reaktion #65682

ord-6a109ae7194e4a79adaf25d9e834a073

Reaktionsgleichung

Cl
hydrochloric acid
O=C([O-])[O-].[K+].[K+]
potassium carbonate
CC(C)=CCBr
3,3-dimethylallyl bromide
Sc1cccc(Br)c1
3-bromothiophenol
CC(C)=CCSc1cccc(Br)c1
m-bromophenyl 3-methyl-2-butenyl sulfide
Ausbeute 98.0%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturwhile cooling
  2. 2
    Extraktionextracted with ether
  3. 3
    SonstigeThe yellow-brown oil obtained
  4. 4
    Sonstigeafter evaporation
  5. 5
    workup.DISTILLATIONwas distilled in a high vacuum

Vorschrift

36 g of 3-bromothiophenol were dissolved in 400 ml of dimethylformamide. After the addition of 27 g of finely powdered potassium carbonate and 29 g of 3,3-dimethylallyl bromide, the mixture was stirred at room temperature for 1 hour, diluted with 500 ml of water, acidified with 3N hydrochloric acid while cooling and extracted with ether. The yellow-brown oil obtained after evaporation was distilled in a high vacuum. There were obtained 48 g of m-bromophenyl 3-methyl-2-butenyl sulfide as a colorless liquid, boiling point 85° C./13.3 Pa.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05420273uspto-grants-1995_05