Methyl iodide → 2,4-Dichloro-6-methoxybenzaldehyde

HRID 1048031Notes

Reaction equation

HRID 1048031 reaction equation
[Cl:1][C:2]1[CH:9]=[C:8]([Cl:10])[CH:7]=[C:6]([OH:11])[C:3]=1[CH:4]=[O:5].[C:12](=O)([O-])[O-].[K+].[K+].IC>CN(C)C=O.O>[Cl:1][C:2]1[CH:9]=[C:8]([Cl:10])[CH:7]=[C:6]([O:11][CH3:12])[C:3]=1[CH:4]=[O:5]

Participants

6

Procedure

To a stirred solution of 2,4-dichloro-6-hydroxybenzaldehyde (1.85 g, 9.69 mmol) in N,N-dimethylformamide (20 mL) at ambient temperature was added solid potassium carbonate (1.47 g, 10.7 mmol), and the resulting yellow mixture was stirred at ambient temperature for 30 minutes. Iodomethane (2.42 mL, 38.7 mmol) was added, and the resulting mixture was stirred in an oil bath set to 50° C. for 30 minutes. The mixture was cooled to ambient temperature and diluted with water (200 mL). After stirring for 10 minutes, the precipitate that formed was collected by filtration, washed with water, and dried under vacuum to afford 2,4-dichloro-6-methoxybenzaldehyde as an off-white powder (1.93 g, 97% yield).

Workup

  1. stirringthe resulting mixture was stirred in an oil bath
  2. waitset to 50° C. for 30 minutes
  3. temperatureThe mixture was cooled to ambient temperature
  4. stirringAfter stirring for 10 minutes
  5. customthe precipitate that formed
  6. filtrationwas collected by filtration
  7. washwashed with water
  8. customdried under vacuum

Sources & evidence

ORD record
ord-593b34ca6c54483d8cc13664b47b8fa1
Source dataset
uspto-grants-2013_10
Patent number
US08569522B2

Reaction notes

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