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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 458512Generated: October 30, 2026

Azobisisobutyronitrile → 4-(2-Methoxyphenyl)benzyl bromide

https://huagongshe.com/reaction/458512

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
Reactant2-Methoxy-4'-methyl-1,1'-biphenylHCID 10313541—
SolventCarbon TetrachlorideHCID 5943—
Product4-(2-Methoxyphenyl)benzyl bromideHCID 21904136—

Reaction Steps

2-methoxy-4′-methylbiphenyl, 160 mg (0.81 mmol), NBS, 158 mg (0.91 mmol), and AIBN, 1 mg (0.006 mmol) were suspended in 7 mL tetrachloromethane, and refluxed for 24 hours. The product was filtered, and the solvent removed from the filtrate by rotary evaporation. Equal amounts of diethyl ether and water were added and the product extracted. The ether layer was separated and dried over MgSO4, filtered, and the solvent removed. 4-(2-Methoxyphenyl)benzyl bromide, 128 mg, was obtained as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07192918B2
Source datasetuspto-grants-2007_03
ORD IDord-d5ec89be604148009bd67110a711d7e4
Source noteuspto-grants-2007_03