Methyl iodide → 2,4-Dichloro-6-methoxybenzaldehyde
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
- stirringthe resulting mixture was stirred in an oil bath
- waitset to 50° C. for 30 minutes
- temperatureThe mixture was cooled to ambient temperature
- stirringAfter stirring for 10 minutes
- customthe precipitate that formed
- filtrationwas collected by filtration
- washwashed with water
- customdried under vacuum
Sources & evidence
- ORD record
- ord-30e40145536d4259b25e1c3be2efbe89
- Source dataset
- uspto-grants-2014_05
- Patent number
- US08716498B2
Reaction notes
Loading…