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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 851513Generated: October 29, 2026

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

https://huagongshe.com/reaction/851513

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 numberUS04385070
Source datasetuspto-grants-1983_05
ORD IDord-74ebfe40f95c4b5ab96068132f0d2dda
Source noteuspto-grants-1983_05