Dimethylformamide → 2-Benzyloxy-3-(dimethylamino)acrolein

[(2,2-Diethoxyethoxy)methyl]benzene (8.30 g, 37.0 mmol) stirred under ice cooling was added with phosphorus pentachloride (8.09 g, 38.8 mmol) over 15 minutes. The mixture was stirred at the same temperature for 15 minutes, and then heated and stirred on an oil bath at 75° C. for 75 minutes. The reaction mixture was cooled by stirring at room temperature for 20 minutes, and then added with anhydrous N,N-dimethylformamide (8.6 mL, 111 mmol) at the same temperature, and the mixture was stirred at room temperature for 3 days. The reaction mixture was added with 8 M aqueous sodium hydroxide on an ice bath until pH became 8 or higher, and then the mixture was diluted with water, and extracted with ether. The organic layer was washed successively with water and saturated brine, dried over anhydrous sodium sulfate, and then concentrated under reduced pressure, and the resulting residue was purified by silica gel column chromatography (hexane:acetone=4:1→2:1) to obtain 2-(benzyloxy)-3-(dimethylamino)acrylaldehyde (4.05 g, 53%) as a brown oil.

1. temperatureheated
2. stirringstirred on an oil bath at 75° C. for 75 minutes
3. temperatureThe reaction mixture was cooled
4. stirringby stirring at room temperature for 20 minutes
5. stirringthe mixture was stirred at room temperature for 3 days
6. extractionextracted with ether
7. washThe organic layer was washed successively with water and saturated brine
8. dry with materialdried over anhydrous sodium sulfate
9. concentrationconcentrated under reduced pressure
10. customthe resulting residue was purified by silica gel column chromatography (hexane:acetone=4:1→2:1)

ORD record

ord-b8ee36f3734e44ba98d59c179fd66a50

Source dataset

uspto-grants-2010_02

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07659271B2