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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1391793Generated: November 3, 2026

3-bromo-N-methoxy-N,2-dimethylbenzamide → 1-(3-Bromo-2-methylphenyl)-1-pentanone

https://huagongshe.com/reaction/1391793

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-bromo-N-methoxy-N,2-dimethylbenzamideHCID 21886197—
ReactantHCID 178418265HCID 178418265—
SolventTetrahydrofuranHCID 8028—
Product1-(3-Bromo-2-methylphenyl)-1-pentanoneHCID 5862989728%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 3-bromo-N,2-dimethyl-N-(methyloxy)benzamide (2.55 g, 9.88 mmol) in anhydrous THF (28 mL) under nitrogen at −78° C. was added a butylmagnesium chloride (20% wt in THF/toluene, 6.94 mL, 11.90 mmol) drop-wise over 15 min. The resulting solution was stirred at −78° C. for 1 h, was allowed to warm to 0° C. and then stirred with slow warming to ambient temperature over 20 h. The reaction was then quenched with water (50 mL) and extracted with EtOAc (2×60 mL). Some saturated aqueous NH4Cl was added to disperse the emulsion formed. The resulting organic layer was then washed with brine (100 mL), dried (Na2SO4), filtered and reduced under vacuum. Purification by SPE (silica, 50 g cartridge), eluting with cyclohexane:EtOAc (gradient 49:1 to 9:1) afforded the title compound as a colourless oil (706 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07338960B2
Source datasetuspto-grants-2008_03
ORD IDord-e4860e1aa2e9417da1cf71ecb4a48891
Source noteuspto-grants-2008_03