Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 604173Generated: October 29, 2026

Azobisisobutyronitrile → 1-Bromo-2-bromomethyl-4-methoxy-5-trifluoromethyl-benzene

https://huagongshe.com/reaction/604173

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
ReactantBenzene, 1-bromo-4-methoxy-2-methyl-5-(trifluoromethyl)-HCID 66602689—
SolventCarbon TetrachlorideHCID 5943—
Product1-Bromo-2-bromomethyl-4-methoxy-5-trifluoromethyl-benzeneHCID 6660268156.6%

Reaction Steps

1-Bromo-4-methoxy-2-methyl-5-trifluoromethyl-benzene (1.0 g), 2,2′-azobisisobutyronitrile (61 mg) and N-bromosuccinimide (795 mg) are dissolved in carbon tetrachloride (15 ml) and the mixture is heated under reflux overnight. The reaction solution is cooled to room temperature and concentrated under reduced pressure. The resulting residue is purified by silica gel column chromatography (hexane:ethyl acetate=1:0→9:1) to give 1-bromo-2-bromomethyl-4-methoxy-5-trifluoromethyl-benzene (732 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07906517B2
Source datasetuspto-grants-2011_03
ORD IDord-f1b129f991ae467882171b2908f2b386
Source noteuspto-grants-2011_03