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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 489477Generated: October 28, 2026

Bromide ion → 2-(2,4-Difluorophenyl)-1-(4-iodophenyl)ethanone

https://huagongshe.com/reaction/489477

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromide ionHCID 259—
Reactant1-(Bromomethyl)-2,4-difluorobenzeneHCID 90297—
Reactant4-Iodo-N-methoxy-N-methyl-benzamideHCID 5461756—
ReactantMagnesiumHCID 5462224—
SolventDiethyl EtherHCID 3283—
Product2-(2,4-Difluorophenyl)-1-(4-iodophenyl)ethanoneHCID 17892897—

Reaction Steps

2,4-Difluorobenzyl bromide (23.7 ml, 0.114 mol) was added dropwise to a stirred mixture of magnesium turnings (8.1 g, 0.183 mol) in dry ether (300 ml) under nitrogen. The mixture was warmed initially until reaction started, and thereafter the bromide was added at such a rate as to maintain a gentle reflux. After 1 hour, the resulting solution of the Grignard reagent was added dropwise at −78° C. to a solution of O,N-dimethyl-4-iodobenzenehydroxamic acid [see step (a)] (45.7 g, 0.157 mol) in dry ether (300 ml), and the mixture was allowed to warm slowly to room temperature overnight. The mixture was partitioned between saturated aqueous ammonium chloride and ethyl acetate, and the organic solution was separated, dried (MgSO4) and concentrated under reduced pressure, to give the title compound as a white solid, 38.71 g (69%), which was characterised by 1H-N.M.R. spectroscopy.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06977302B2
Source datasetuspto-grants-2005_12
ORD IDord-eb7ad85e24eb4ac281a4e671ea74b5a5
Source noteuspto-grants-2005_12