Hydrogen Peroxide → 3-Chloro-2-fluorobenzoic acid

HRID 2386202Notes

Reaction equation

HRID 2386202 reaction equation
[Cl:1][C:2]1[C:3]([F:10])=[C:4]([CH:7]=[CH:8][CH:9]=1)[CH:5]=[O:6].[OH-:11].[Na+].OO>C(O)(C)(C)C>[Cl:1][C:2]1[C:3]([F:10])=[C:4]([CH:7]=[CH:8][CH:9]=1)[C:5]([OH:11])=[O:6]

Participants

5

Conditions

Temperature
50 °C

Procedure

3-Chloro-2-fluorobenzaldehyde (15.9 g, 0.1 mol) was dissolved in tert-butanol (60 ml), stirred and heated under N2 at 50° C. 2M aqueous NaOH (100 ml, 0.2 mol) was warmed to 50° C. and added to the solution of the aldehyde. Aqueous hydrogen peroxide solution (H2O2, 30%, 70 ml, 0.6 mol) was added over 45 min, maintaining the temperature at 55-60° C. The mixture was stirred and heated under N2 for a further 1 h, cooled and concentrated in vacuo. The residual slurry was filtered. The filtrate was washed with toluene (2×xx ml) and acidified to pH 1 with 5N hydrochloric acid whilst stirring vigorously. The resulting solid was collected by filtration, washed with water and dried in vacuo at 50° C. to give 11.1 g of product, mp 179-181° C.

Workup

  1. temperaturemaintaining the temperature at 55-60° C
  2. stirringThe mixture was stirred
  3. temperatureheated under N2 for a further 1 h
  4. temperaturecooled
  5. concentrationconcentrated in vacuo
  6. filtrationThe residual slurry was filtered
  7. washThe filtrate was washed with toluene (2×xx ml)
  8. stirringwhilst stirring vigorously
  9. filtrationThe resulting solid was collected by filtration
  10. washwashed with water
  11. customdried in vacuo at 50° C.

Sources & evidence

ORD record
ord-e7f8a5fd191542f397be6c3e003730a7
Source dataset
uspto-grants-2012_09
Patent number
US08268823B2

Reaction notes

Loading…