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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 965978Generated: October 30, 2026

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

https://huagongshe.com/reaction/965978

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 numberUS06951876B2
Source datasetuspto-grants-2005_10
ORD IDord-9bbc321a1af34c72b0bf2f34c9eea19e
Source noteuspto-grants-2005_10