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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1476747Generated: October 30, 2026

2-Bromo-1,4-difluorobenzene → 4-Chloro-1-(2,5-difluorophenyl)butan-1-one

https://huagongshe.com/reaction/1476747

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-1,4-difluorobenzeneHCID 67862—
Reactant4-chloro-N-methoxy-N-methylbutyramideHCID 11252200—
ReactantHCID 178418918HCID 178418918—
SolventTetrahydrofuranHCID 8028—
Product4-Chloro-1-(2,5-difluorophenyl)butan-1-oneHCID 6581142166.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

2-Bromo-1,4-difluorobenzene (53.6 g, 277.74 mmol) in THF cooled to −50° C. was added to isopropyl magnesium chloride (2M in THF) (133 mL, 266 mmol). The reaction mixture thus obtained was warmed to 0° C. and stirred for 1 h. The reaction mixture was cooled again to −50° C. 4-chloro-N-methoxy-N-methylbutanamide (40 g, 241.52 mmol) in THF (200 mL) was added dropwise to this reaction mixture with stirring and the stirring was continued at 0° C. for 1 h. The reaction mixture was quenched with saturated aqueous NH4Cl solution, extracted with ethylacetate. The organic layer collected was washed with water (500 mL) and then with brine solution, dried over anhydrous sodium sulfate and concentrated under reduced pressure to afford a crude liquid residue. The residue thus obtained was purified by column chromatography (using 60-120 silica gel and 5% EtOAc in Hexane as eluent) to afford 35 g of the title compound as a colourless liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09402833B2
Source datasetuspto-grants-2016_08
ORD IDord-e4b8161ba3bc49b6a784d3d124a09269
Source noteuspto-grants-2016_08