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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2194682Generated: October 26, 2026

Hydrogen Bromide → 2-Bromo-1-(2-fluorophenyl)-2-(phenylthio)ethanone

https://huagongshe.com/reaction/2194682

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
Reactant1-(2-Fluorophenyl)-2-(phenylthio)ethanoneHCID 43413345—
CatalystCopper bromide (CuBr2)HCID 24611—
SolventAcetic AcidHCID 176—
SolventEthyl AcetateHCID 8857—
Product2-Bromo-1-(2-fluorophenyl)-2-(phenylthio)ethanoneHCID 5944873492%

Reaction Steps

To a solution of 1-(2-fluorophenyl)-2-(phenylthio)ethanone (413 mg) in ethyl acetate (6 mL) were added copper (II) bromide (419 mg) and a 47% solution (2 drops) of hydrogen bromide in acetic acid and the mixture was stirred at 80° C. for 2 hr. The reaction mixture was cooled to room temperature, and concentrated under reduced pressure. A saturated aqueous sodium hydrogen carbonate solution was added to the residue, and the mixture was extracted with ethyl acetate. The extract was washed with saturated aqueous sodium hydrogen carbonate solution, water and saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure to give the title compound as a brown oil (yield 503 mg, yield 92%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08334301B2
Source datasetuspto-grants-2012_12
ORD IDord-e0323f0406d444b8bd7ec443a8e870be
Source noteuspto-grants-2012_12