Reaktion #65896

ord-8661317d4f8d49b68db114f65a279bdf

Reaktionsgleichung

BrBr
bromine
Cc1ccc(B(O)O)cc1
4-methylphenylboronic acid
BrBr
bromine
O
water
O
water
OB(O)c1ccc(CBr)cc1
4-bromomethylphenylboronic acid
Ausbeute 67.5%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturwas heated
  2. 2
    Sonstigewas collected
  3. 3
    Sonstigea crystalline slurry was formed
  4. 4
    Temperaturto cool
  5. 5
    FiltrationThe suspended solid was collected by filtration
  6. 6
    Waschenwashed with methyl chloroform (2×50 ml)
  7. 7
    Sonstigedried at ambient temperature

Vorschrift

A mixture of 4-methylphenylboronic acid (27.2 g; 0.2 mole) in methyl chloroform (250 ml) was heated at reflux with azeotropic removal of water until approximately 2.5 ml of water was collected and a crystalline slurry was formed. A solution of azo(bisisobutyronitrile) (1.0 g) and bromine (32 g) in methyl chloroform (25 ml) was added to the refluxing slurry over 2-3 hours. The mixture was then refluxed until the bromine colour was discharged. The reaction mixture was allowed to cool and stirred at 10°-15° C. for 30 minutes. The suspended solid was collected by filtration, washed with methyl chloroform (2×50 ml) and dried at ambient temperature to give the anhydride of 4-bromomethylphenylboronic acid (29 g) (Compound F) as a white, crystalline solid, which was used without further purification or characterisation.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05420292uspto-grants-1995_05