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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1739502Generated: November 2, 2026

4-Bromotoluene → 4-Bromobenzyl bromide

https://huagongshe.com/reaction/1739502

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromotolueneHCID 7805—
ReactantN-bromobutanimideHCID 67184—
SolventCarbon TetrachlorideHCID 5943—
Product4-Bromobenzyl bromideHCID 6852759.3%

Reaction Steps

To a suspension of 4-bromotoluene (60 g) and N-bromosuccinimide (69 g) in carbon tetrachloride (300 ml) was added 2,2'-azobis(isobutylonitrile) (0.1 g). The resulting mixture was heated under reflux for 2 hours. After the reaction mixture was cooled, succinimide so precipitated was removed by filtration, and the filtrate was washed with saturated aqueous sodium hydrogencarbonate. The organic layer was dried over anhydrous magnesium sulfate, followed by removal through distillation. The oily substance so obtained was crystallized from n-hexane, whereby 52 g of the title compound was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05965738
Source datasetuspto-grants-1999_10
ORD IDord-2cee7facc5384698845343dd65382108
Source noteuspto-grants-1999_10