Dimethylformamide → 2-(2-Methoxyethyl)-6-methylbenzaldehyd

To a stirred solution of 2-(2-bromo-3-methylphenyl)ethyl methylether (1.5 g, 6.5 mmol) in anhydrous tetrahydrofuran (10 ml) was added magnesium (turnings) (0.16 g, 6.6 mmol). The mixture was refluxed in a nitrogen atmosphere until the reaction started and then stirred without heating for 15 min. The mixture was stirred at 50° C. overnight. The mixture was cooled to room temperature and N,N-dimethylformamide (0.7 g) was added and the mixture was stirred for 30 min. A saturated ammonium chloride solution (10 ml) was added and the mixture was stirred for 1 h. at room temperature. Toluene (20 ml) was added and the organic layer was separated, dried (Na2SO4) and evaporated under reduced pressure. The residue was purified by column chromatography on silica gel using methylene chloride as eluent to separate the lipophilic biproducts and methylene chloride/diethyl ether (7:3) as eluent to isolate (0.17 g, (15%) of the title compound as an oil.

1. temperatureThe mixture was refluxed in a nitrogen atmosphere until the reaction
2. temperaturewithout heating for 15 min
3. stirringThe mixture was stirred at 50° C. overnight
4. stirringthe mixture was stirred for 30 min
5. stirringthe mixture was stirred for 1 h. at room temperature
6. customthe organic layer was separated
7. dry with materialdried (Na2SO4)
8. customevaporated under reduced pressure
9. customThe residue was purified by column chromatography on silica gel
10. customto separate the lipophilic biproducts and methylene chloride/diethyl ether (7:3) as eluent

ORD record

ord-270ef70aa8df41b3a24d4db0508f5b6f

Source dataset

uspto-grants-2004_09

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US06790960B2