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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1754935Generated: October 28, 2026

Acetamide, N-(3,5-dimethylphenyl)- → N-(4-bromo-3,5-dimethylphenyl)acetamide

https://huagongshe.com/reaction/1754935

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetamide, N-(3,5-dimethylphenyl)-HCID 74903—
ReactantBenzyltrimethylammoniumtribromideHCID 53442637—
SolventDichloromethane methanolHCID 21226129—
ProductN-(4-bromo-3,5-dimethylphenyl)acetamideHCID 424625090%

Reaction Steps

Benzyltrimethylammonium tribromide (BTMA-Br3) (7.8 g, 20.21 mmol) was added to a solution of N-(3,5-dimethyl-phenyl)-acetamide (3.0 g, 18.38 mmol) in CH2Cl2/MeOH (90 ml/90 ml) at room temperature in an Ar atmosphere. The reaction mixture was stirred at room temperature for 10 minutes. The reaction mixture was concentrated under reduced pressure, and CH2Cl2 was then added to the resulting residue. The organic layer was washed with H2O, and then dried over anhydrous Na2SO4 and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:EtOAc=1:1) to give N-(4-bromo-3,5-dimethyl-phenyl)-acetamide (4.0 g, yield 90%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09169254B2
Source datasetuspto-grants-2015_10
ORD IDord-377a7f6a6e6547a096434dc56397f3d7
Source noteuspto-grants-2015_10