Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 434539Generated: October 25, 2026

p-Fluorotoluene → 4-Fluorobenzyl bromide

https://huagongshe.com/reaction/434539

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-FluorotolueneHCID 9603—
ReactantN-bromobutanimideHCID 67184—
CatalystBenzoyl PeroxideHCID 7187—
SolventCarbon TetrachlorideHCID 5943—
Product4-Fluorobenzyl bromideHCID 68021101.1%

Reaction Steps

A 300-ml flask was charged with 16.6 g of 4-fluorotoluene, 30.0 g of NBS, 0.5 g of benzoyl peroxide and 150 ml of carbon tetrachloride, and the mixture was refluxed for 2.0 hours. The reaction mixture was cooled to room temperature, and the formed precipitate was removed by filtration and the residual CCl4 solution was washed with dilute alkali and then with water, dried over Na2SO4, and evaporated under reduced pressure to give 28.8 g of crude 4-fluorobenzyl bromide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04397864
Source datasetuspto-grants-1983_08
ORD IDord-488f31c16d854192accd904c27116779
Source noteuspto-grants-1983_08