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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1369980Generated: October 29, 2026

N-bromobutanimide → 4-(Bromomethyl)-1-fluoro-2-iodobenzene

https://huagongshe.com/reaction/1369980

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant4-Fluoro-3-iodotolueneHCID 232023—
CatalystAzobisisobutyronitrileHCID 6547—
SolventCarbon TetrachlorideHCID 5943—
Product4-(Bromomethyl)-1-fluoro-2-iodobenzeneHCID 1851645551.1%

Reaction Steps

4-Fluoro-3-iodotoluene (50 g, 210 mMol), N-bromosuccinimide (37.7 g, 212 mMol) and 2,2′-azobis-(2-methylpropionitrile) (348 mg, 2.12 mMol) were dissolved in carbon tetrachloride (300 mL) under an atmosphere of dry N2. The mixture was heated to reflux for 4 hours and then cooled to ambient temperature. The mixture was concentrated under vacuum and triturated with Et2O. The filtrate was successively washed with water, aqueous saturated NaHCO3 and brine. The ether layer was dried over MgSO4, filtered and concentrated under vacuum to give a red oil. The oil was chromatographed on flash silica gel eluting with hexanes to give 33.8 g of the titled compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06579887B2
Source datasetuspto-grants-2003_06
ORD IDord-47808013bdee4e72aa7ec309018f45ed
Source noteuspto-grants-2003_06