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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1589455Generated: November 3, 2026

p-Fluorotoluene → 4-Fluorobenzyl bromide

https://huagongshe.com/reaction/1589455

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 numberUS04570005
Source datasetuspto-grants-1986_02
ORD IDord-c435fa6f8fd84a1286a6b069e41db32a
Source noteuspto-grants-1986_02