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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1875146Generated: October 26, 2026

Azobisisobutyronitrile → 2-[(3-Bromo-5-chlorophenyl)oxy]-4-(bromomethyl)-1-chloro-3-fluorobenzene

https://huagongshe.com/reaction/1875146

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
Reactant2-[(3-Bromo-5-chlorophenyl)oxy]-1-chloro-3-fluoro-4-methylbenzeneHCID 68486615—
SolventCarbon TetrachlorideHCID 5943—
Product2-[(3-Bromo-5-chlorophenyl)oxy]-4-(bromomethyl)-1-chloro-3-fluorobenzeneHCID 6848367749%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 2-[(3-bromo-5-chlorophenyl)oxy]-1-chloro-3-fluoro-4-methylbenzene (9.69 g, 27.7 mmol) and NBS (4.93 g, 27.7 mmol) in carbon tetrachloride (250 ml) was added AIBN (0.227 g, 1.384 mmol) and the mixture was stirred at 80° C. overnight. An additional portion of AIBN (0.227 g, 1.384 mmol) was added and the mixture was stirred for another 4 hours. The mixture was cooled to rt, the solvent was removed and the crude material was purified via silica gel chromatography to give 2-[(3-bromo-5-chlorophenyl)oxy]-4-(bromomethyl)-1-chloro-3-fluorobenzene (5.78 g, 49% yield). 1H NMR (400 MHz, DMSO-d6) δ ppm 7.38-7.67 (m, 3H), 7.10 (s, 1H), 6.98-7.07 (m, 1H), 4.70 (s, 2H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304419B2
Source datasetuspto-grants-2012_11
ORD IDord-35b6b1cdcccb4a74a084b82047f071d0
Source noteuspto-grants-2012_11