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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 394871Generated: October 25, 2026

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

https://huagongshe.com/reaction/394871

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromo-N-methoxy-N-methylbenzamideHCID 10999252—
ReactantHCID 178455851HCID 178455851—
SolventTetrahydrofuranHCID 8028—
Product1-Butanone, 1-(4-bromophenyl)-HCID 7868082.1%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06603008B1
Source datasetuspto-grants-2003_08
ORD IDord-075d10107c304e7182c6eb95f615b142
Source noteuspto-grants-2003_08