4-Bromo-N-methoxy-N-methylbenzamide → 1-Butanone, 1-(4-bromophenyl)-

To a solution of 4-bromo-N-methoxy-N-methylbenzamide (13.4 g, 54.2 mmol) in THF (200 ml) was added n-PrMgBr (2M THF solution, 54.0 ml, 108 mmol) at 0° C. The mixture was stirred at room temperature for 45 minutes. Further n-PrMgBr (13.5 ml, 27.0 mmol) was added at 0° C., and the mixture was stirred at room temperature for 30 minutes. The excess reagent was quenched with saturated aqueous NH4Cl (200 ml), and ether (300 ml) was added. The organic layer was separated and the aqueous layer was extracted with ether (300 ml). The combined organic layer was washed with water (200 ml) and brine (200 ml), dried over Na2SO4, and concentrated in vacuo. The obtained residue was chromatographed on a column of silica gel eluting with hexane/ethyl acetate (15:1) to give 10.1 g (82%) of the title compound as a yellow solid.

1. stirringthe mixture was stirred at room temperature for 30 minutes
2. customThe excess reagent was quenched with saturated aqueous NH4Cl (200 ml), and ether (300 ml)
3. additionwas added
4. customThe organic layer was separated
5. extractionthe aqueous layer was extracted with ether (300 ml)
6. washThe combined organic layer was washed with water (200 ml) and brine (200 ml)
7. dry with materialdried over Na2SO4
8. concentrationconcentrated in vacuo
9. customThe obtained residue was chromatographed on a column of silica gel eluting with hexane/ethyl acetate (15:1)

ORD record

ord-18dc0014c15a4c96b72c12622aae81c7

Source dataset

uspto-grants-2005_10

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US06951876B2