Sulfuric Acid → 3-Bromo-4-(trifluoromethoxy)benzaldehyde

HRID 488845Notes

Reaction equation

HRID 488845 reaction equation
[F:1][C:2]([F:13])([F:12])[O:3][C:4]1[CH:11]=[CH:10][C:7]([CH:8]=[O:9])=[CH:6][CH:5]=1.C(Cl)Cl.OS(O)(=O)=O.[Br:22]N1C(=O)CCC1=O>C(O)(C(F)(F)F)=O>[Br:22][C:5]1[CH:6]=[C:7]([CH:10]=[CH:11][C:4]=1[O:3][C:2]([F:12])([F:13])[F:1])[CH:8]=[O:9]

Participants

6

Procedure

To a solution of 4-trifluoromethoxybenzaldehyde (215 g, 1.13 mol) in a mixture of TFA (300 mL), CH2Cl2 (300 mL) and H2SO4 (150 mL) was added at room temperature N-bromosuccinimide (402 g, 2.26 mol) in equal portion over 7 hours. The reaction mixture was stirred for 4 days at room temperature, poured into ice-water and extracted with CH2Cl2. The organic layer was washed with water then treated with saturated NaHCO3 (1.5 L) for 2 hrs. The layers were separated and the organic layer further washed with water and brine, dried over MgSO4, filtered and evaporated. The residue was triturated with hexane and filtered. After evaporation of the solvent, the residue was distilled to give 3-bromo-4-trifluoromethoxybenzaldehyde (190.2 g, 81° C., 1.0 mm/Hg, 62%).

Workup

  1. extractionextracted with CH2Cl2
  2. washThe organic layer was washed with water
  3. additionthen treated with saturated NaHCO3 (1.5 L) for 2 hrs
  4. customThe layers were separated
  5. washthe organic layer further washed with water and brine
  6. dry with materialdried over MgSO4
  7. filtrationfiltered
  8. customevaporated
  9. customThe residue was triturated with hexane
  10. filtrationfiltered
  11. customAfter evaporation of the solvent
  12. distillationthe residue was distilled

Sources & evidence

ORD record
ord-49c668e14dcc40bab5fb23d5a54558e2
Source dataset
uspto-grants-2005_12
Patent number
US06974826B2

Reaction notes

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