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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 394889Generated: October 26, 2026

4-Bromo-3-fluoro-N-methoxy-N-methylbenzamide → 1-(4-Bromo-3-fluorophenyl)butan-1-one

https://huagongshe.com/reaction/394889

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromo-3-fluoro-N-methoxy-N-methylbenzamideHCID 22313823—
ReactantHCID 178455851HCID 178455851—
SolventTetrahydrofuranHCID 8028—
Product1-(4-Bromo-3-fluorophenyl)butan-1-oneHCID 2231384081.7%

Reaction Steps

To a stirred solution of 4-Bromo-3-fluoro-N-methoxy-N-methylbenzamide (3.0 g, 12.19 mmol) in tetrahydrofuran (35 ml) was added 2M n-propylmagnesium bromide (12.2 ml, 24.38 mmol) dropwise under nitrogen at 0° C. The reaction mixture was stirred at room temperature for 2 h. This was quenched by sat. ammonium chloride and stirred at rt for 30 min. The organic layer was separated and the aqueous layer was extracted with ethyl acetate. The extracts was dried (MgSO4) and concentrated. This was purified on silica gel eluting with ethyl acetate/hexane (1:10) to afford 2.44 g (81.7%) of the titled compound as a slight yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06603008B1
Source datasetuspto-grants-2003_08
ORD IDord-ba47e843e9114b0ea614bbaad30cd6a2
Source noteuspto-grants-2003_08