Methane → 4-Bromo-2-formylbenzoic acid

HRID 1047857Notes

Reaction equation

HRID 1047857 reaction equation
Br[CH:2]1[C:10]2[C:5](=[CH:6][CH:7]=[C:8]([Br:11])[CH:9]=2)[C:4](=[O:12])[O:3]1.[OH-:13].[Na+].C>O>[Br:11][C:8]1[CH:7]=[CH:6][C:5]([C:4]([OH:3])=[O:12])=[C:10]([CH:2]=[O:13])[CH:9]=1

Participants

5

Conditions

Temperature
80 °C

Procedure

The mixture of 3,5-dibromo-3H-isobenzofuran-1-one (B3) (38 g, 130 mmol) in a solution of 10N NaOH (28.6 mL, 286 mmol) and water (240 mL) is heated for 2 h at 80° C. Activated charcoal (2 g) is added and the mixture is refluxed for another 1 hour. Mixture is hot filtered and acidified with 2N methanesulfonic acid (100 mL). The resulting mixture is cooled in an ice-water bath for 1 h. The solid is filtered and washed with water (4×25 mL) and vacuum dried under KOH to yield 4-bromo-2-formyl-benzoic acid (C3) (26.5 g, 89%, mp: 202° C.). Recrystallization: Dissolved 4-bromo-2-formyl-benzoic acid (C3) in hot EtOH (220 mL) and cooled the mixture in an ice-water bath for 4 h. The solid is filtered and rinsed with cold EtOH (3×20 mL). The solid is then vacuum dried over KOH to yield 4-bromo-2-formyl-benzoic acid (16.8 g, 63%, mp: 204-205° C.).

Workup

  1. temperaturethe mixture is refluxed for another 1 hour
  2. filtrationMixture is hot filtered
  3. temperatureThe resulting mixture is cooled in an ice-water bath for 1 h
  4. filtrationThe solid is filtered
  5. washwashed with water (4×25 mL) and vacuum
  6. customdried under KOH

Sources & evidence

ORD record
ord-8aa1f99de3874ff896fd2e921ce89ca3
Source dataset
uspto-grants-2013_10
Patent number
US08569535B2

Reaction notes

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