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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 69114Generated: October 29, 2026

Acetonitrile → 1-[2-Amino-5-bromo-4-(trifluoromethyl)phenyl]ethanone

https://huagongshe.com/reaction/69114

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantN-bromobutanimideHCID 67184—
Reactant1-(2-Amino-4-(trifluoromethyl)phenyl)ethan-1-oneHCID 46835500—
SolventDiethyl EtherHCID 3283—
Product1-[2-Amino-5-bromo-4-(trifluoromethyl)phenyl]ethanoneHCID 6669613564.7%

Reaction Steps

To a mixture of 11.6 g of 1-[2-amino-4-(trifluoromethyl)phenyl]ethanone, 60 mL of acetonitrile, and 230 mL of diethyl ether was added 2.85 g of Amberlyst (registered trademark) 15, and 10.1 g of N-bromosuccinimide was added thereto in three times in an ice bath. After stirring for 30 minutes in an ice bath, the mixture was stirred at room temperature overnight. The insoluble material was filtered and washed with ethyl acetate. To the filtrate were added water and ethyl acetate, and the aqueous layer was separated. The organic layer was washed with a 10% aqueous sodium thiosulfate solution and saturated brine, and dried over anhydrous magnesium sulfate, and then solvent was evaporated. The residue was purified by silica gel column chromatography (n-hexane/ethyl acetate) to obtain 10.36 g of 1[2-amino-5-bromo-4-(trifluoromethyl)phenyl]ethanone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822448B2
Source datasetuspto-grants-2014_09
ORD IDord-195fbe543fdd481195764ad9f4a660d0
Source noteuspto-grants-2014_09