Reaktion #955968

ord-69a47141d8424544aa5db2c65d113327

Reaktionsgleichung

Clc1ccc(Cl)cc1
dichlorobenzene
CCCCC(CC)[CH2][Mg][Br]
(2-ethylhexyl)magnesium bromide
CCCCC(CC)Cc1ccccc1CC(CC)CCCC
product
Ausbeute 21.0%
CCCCC(CC)Cc1ccccc1CC(CC)CCCC
1,2-bis(2-ethylhexyl)benzene
Ausbeute 21.0%

Lösungsmittel

Reaktionsbedingungen

Temperatur
0°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeA dry 1 L three-neck round bottom flask, equipped with a condenser and an addition funnel
  2. 2
    workup.ADDITIONAfter addition
  3. 3
    Temperaturthe reaction was heated
  4. 4
    Temperaturto reflux for 12 hours
  5. 5
    Temperaturcooled down to room temperature
  6. 6
    ExtraktionThe mixture was extracted with MTBE (3×100 mL)
  7. 7
    Trocknendried over anhydrous MgSO4
  8. 8
    Filtrationfiltered
  9. 9
    Sonstigethe solvent was removed by rotary evaporation
  10. 10
    workup.DISTILLATIONThe mixture was purified by distillation under a reduced pressure

Vorschrift

A dry 1 L three-neck round bottom flask, equipped with a condenser and an addition funnel, was charged with Ni(dppp)2Cl2 (0.99 g, 1.83 mmol) and dichlorobenzene (26.7 g, 182 mmol). The reaction solution was cooled down to 0° C. and then (2-ethylhexyl)magnesium bromide solution (400 mmol) was added dropwise via the addition funnel under nitrogen. After addition was complete, the reaction was heated to reflux for 12 hours and then cooled down to room temperature. The reaction solution was poured into 100 mL of DI water. The mixture was extracted with MTBE (3×100 mL). The organic phase was combined, dried over anhydrous MgSO4, filtered and the solvent was removed by rotary evaporation. The mixture was purified by distillation under a reduced pressure to give the product (11.5 g, 21%) as colorless oil.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08968885B2uspto-grants-2015_03