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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1099132Generated: November 3, 2026

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

https://huagongshe.com/reaction/1099132

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, 0.2 mmol). 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 numberUS08143298B2
Source datasetuspto-grants-2012_03
ORD IDord-7173e65fde9a4a7a9696849d317652b2
Source noteuspto-grants-2012_03