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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1895507Generated: November 2, 2026

Benzoyl Peroxide → 5-(4'-(Bromomethyl)(1,1'-biphenyl)-2-yl)-1-trityl-1H-tetraazole

https://huagongshe.com/reaction/1895507

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
Reactant5-(4'-Methyl-(1,1'-biphenyl)-2-yl)-1-trityl-1H-tetrazoleHCID 10152019—
SolventDichloromethaneHCID 6344—
Product5-(4'-(Bromomethyl)(1,1'-biphenyl)-2-yl)-1-trityl-1H-tetraazoleHCID 10053461—

Reaction Steps

To a nitrogen-saturated suspension of N-triphenylmethyl-5-[4′-methylbiphenyl-2-yl]tetrazole (10 g, 20.9 mmol) in DCM was added NBS (3.7 g, 20.9 mmol) and a catalytic amount of benzoyl peroxide (60 mg, 240 μmol). The mixture was stirred at reflux for 15 hours. After cooling to room temperature, the precipitate was filtered and the organic solution was concentrated in vacuo. Silica gel chromatography (EtOAc/hexane) gave the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08513432B2
Source datasetuspto-grants-2013_08
ORD IDord-2e953260f64f4edcb0755d83e0f16be7
Source noteuspto-grants-2013_08