Methane, dichloromethoxy- → 4-broMo-2-fluoro-5-Methoxy-benzaldehyde

HRID 879013Notes

Reaction equation

HRID 879013 reaction equation
[Br:1][C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[CH:4][C:3]=1[O:9][CH3:10].[CH3:11][O:12]C(Cl)Cl>[Ti](Cl)(Cl)(Cl)Cl.C(Cl)(Cl)Cl>[Br:1][C:2]1[C:3]([O:9][CH3:10])=[CH:4][C:5]([CH:11]=[O:12])=[C:6]([F:8])[CH:7]=1

Participants

5

Conditions

Temperature
0 °C

Procedure

To a mixture of 2-bromo-4-fluoro-1-methoxybenzene (4.10 g) and titanium tetrachloride (4.4 mL), dichloromethyl methyl ether (3.5 mL) was added under ice cooling, and then the reaction mixture was stirred at 0° C. for 2.5 hours. To the reaction mixture was added chloroform, and the reaction mixture was poured into ice water, and then stirred at room temperature for 1 hour. The organic layer was separated and dried over anhydrous sodium sulfate, filtered, and the filtrate was concentrated under reduced pressure. The obtained residue was added hexane and the produced solid was filtered to give the titled compound (1.61 g) as a white solid.

Workup

  1. additionwas added under ice cooling
  2. stirringstirred at room temperature for 1 hour
  3. customThe organic layer was separated
  4. dry with materialdried over anhydrous sodium sulfate
  5. filtrationfiltered
  6. concentrationthe filtrate was concentrated under reduced pressure
  7. additionThe obtained residue was added hexane
  8. filtrationthe produced solid was filtered

Sources & evidence

ORD record
ord-b5a6b0b06af844f4846de76f0ebc5d7e
Source dataset
uspto-grants-2015_03
Patent number
US08987473B2

Reaction notes

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