Water → 4-Bromo-3-fluorobenzoic acid

HRID 379033Notes

Reaction equation

HRID 379033 reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH3:8])=[CH:4][C:3]=1[F:9].N1C=CC=CC=1.[Mn]([O-])(=O)(=O)=[O:17].[K+].[OH2:22]>>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]([OH:17])=[O:22])=[CH:4][C:3]=1[F:9]

Participants

5

Procedure

4-Bromo-3-fluorotoluene (40.0 g, 0.212 mol) was heated at 90° C. in H2O (200 mL) and pyridine (200 mL) with mechanical stirring under Ar. Potassium permanganate (KMnO4) (67 g, 0.424 mol) was added portionwise over 3 h. After 4 h, an HPLC of a filtered sample indicated 50% conversion to the acid. An additional 30 g of KMnO4 was added and heating continued overnight. HPLC indicated 81% conversion. Further KMnO4 was added portionwise with reaction monitoring by HPLC until >95% conversion was obtained. The reaction mixture was filtered through Celite, the filter pad washed with H2O, aq NaOH and EtOH. The filtrate was concentrated to a small volume, then partitioned between 3N NaOH solution and diethyl ether. The aqueous basic layer was separated, cooled in an ice-H2O bath and acidified slowly with 6N HCl solution to precipitate the white solid product. This was collected by suction filtration and dried at 40° C. in a vacuum oven overnight to give the title compound. mp 190-192° C.

Workup

  1. temperatureheating continued overnight
  2. customwas obtained
  3. filtrationThe reaction mixture was filtered through Celite
  4. washthe filter pad washed with H2O, aq NaOH and EtOH
  5. concentrationThe filtrate was concentrated to a small volume
  6. custompartitioned between 3N NaOH solution and diethyl ether
  7. customThe aqueous basic layer was separated
  8. temperaturecooled in an ice-H2O bath
  9. customto precipitate the white solid product
  10. filtrationThis was collected by suction filtration
  11. customdried at 40° C. in a vacuum oven overnight

Sources & evidence

ORD record
ord-cf6b102074304cfb92900f12fc8e9499
Source dataset
uspto-grants-2001_10
Patent number
US06297239B1

Reaction notes

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