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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1648230Generated: November 2, 2026

Bromine → 3-Bromo-3-(2-chlorophenyl)-1,1,1-trifluoro-2-propanone

https://huagongshe.com/reaction/1648230

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
Reactant3-(2-Chlorophenyl)-1,1,1-trifluoropropan-2-oneHCID 2781549—
ReactantSodium BisulfiteHCID 23665763—
SolventCarbon TetrachlorideHCID 5943—
Product3-Bromo-3-(2-chlorophenyl)-1,1,1-trifluoro-2-propanoneHCID 1528993232.1%

Reaction Steps

2.0 g (9.0 mmole) of 1-(2-chlorophenyl)-3,3,3-trifluoro-2-propanone were dissolved in 30 ml of carbon tetrachloride, and then 0.46 ml (9.0 mmole) of bromine was added to the solution, which was then stirred at room temperature for 10 hours. At the end of this time, sodium hydrogensulfite was added to the reaction mixture, and the mixture was stirred at room temperature for 15 minutes, after which insolubles were removed by filtration. The filtrate was concentrated by evaporation under reduced pressure, and the residue was subjected to silica gel column chromatography, using a 10:2 by volume mixture of toluene and ethyl acetate as the eluent, to give 0.87 g of the title compound as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05436242
Source datasetuspto-grants-1995_07
ORD IDord-c9ecb53cacd1462dae2e2ec9f2d68988
Source noteuspto-grants-1995_07