Water → 4-(Bromomethyl)phenylboronic acid

HRID 37618

Reaction equation

HRID 37618 reaction equation
[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([B:8]([OH:10])[OH:9])=[CH:4][CH:3]=1.O.[Br:12]Br>CC(Cl)(Cl)Cl.N(C(C)(C)C#N)=NC(C)(C)C#N>[Br:12][CH2:1][C:2]1[CH:7]=[CH:6][C:5]([B:8]([OH:10])[OH:9])=[CH:4][CH:3]=1

Participants

6

Procedure

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.

Workup

  1. temperaturewas heated
  2. customwas collected
  3. customa crystalline slurry was formed
  4. temperatureto cool
  5. filtrationThe suspended solid was collected by filtration
  6. washwashed with methyl chloroform (2×50 ml)
  7. customdried at ambient temperature

Sources & evidence

ORD record
ord-8661317d4f8d49b68db114f65a279bdf
Source dataset
uspto-grants-1995_05
Patent number
US05420292

Linked notes

Loading…