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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1153714Generated: November 1, 2026

Benzoyl Peroxide → 1-(Bromomethyl)-4-fluoro-2-nitrobenzene

https://huagongshe.com/reaction/1153714

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
Reactant4-Fluoro-2-nitrotolueneHCID 67965—
SolventCarbon TetrachlorideHCID 5943—
Product1-(Bromomethyl)-4-fluoro-2-nitrobenzeneHCID 12761379—

Reaction Steps

A mixture of 2-nitro-4-fluorotoluene (1.65 g), N-bromo-succinimide (1.78 g), carbon tetrachloride 10.0 ml) and benzoyl peroxide (0.1 g) was heated at the reflux temperature until the solid residue was observed to be floating at the surface (ca. 3 hours). After removing the solid by filtration, the filtrate was diluted with diethyl ether, washed with water, dried over anhydrous magnesium sulphate and concentrated by evaporation of the solvents under reduced pressure. The residue (estimated to contain ca. 35% w/w of the benzyl bromide in admixture with unchanged starting material) was subjected to column chromatography using a silica column and diethyl ether/petroleum ether (ratio 1:9 v/v) as eluent to yield pure 2-nitro-4-fluorobenzyl bromide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04486355
Source datasetuspto-grants-1984_12
ORD IDord-58e633862e3a4f13ba7afcd7dc04053b
Source noteuspto-grants-1984_12