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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2039414Generated: October 31, 2026

N-bromobutanimide → 4-Bromo-1-(bromomethyl)-2-iodobenzene

https://huagongshe.com/reaction/2039414

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant4-Bromo-2-iodo-1-methylbenzeneHCID 15442947—
CatalystBenzyl PeroxideHCID 11229634—
SolventChlorobenzeneHCID 7964—
Product4-Bromo-1-(bromomethyl)-2-iodobenzeneHCID 5323130724.2%

Reaction Steps

N-Bromosuccinimide (NBS) (1.1 molar equivalents, 66.5 g, 373 mmol) and benzyl peroxide (0.006 molar equivalent, 450.7 mg, 1.9 mmol) are added to a solution of 2-iodo-4-bromotoluene 6 (1 molar equivalent, 100.3 g, 338 mmol) in chlorobenzene (1200 ml). The batch is then stirred under reflux overnight. After the solvent has been removed in a rotary evaporator, ethyl acetate and water are added. The aqueous phase is extracted by shaking with ethyl acetate. The organic phase is washed by shaking with water, dried and evaporated in a rotary evaporator. The product 7 (30.7 g, 24%) is obtained in the form of a white powder by recrystallisation from ethanol (50 ml).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08580395B2
Source datasetuspto-grants-2013_11
ORD IDord-c1654333ecc6495ebafb0d1456e354dd
Source noteuspto-grants-2013_11