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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1655515Generated: November 2, 2026

N-bromobutanimide → 1,1'-Biphenyl, 4'-(bromomethyl)-2-nitro-

https://huagongshe.com/reaction/1655515

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant4'-Methyl-2-nitro-1,1'-biphenylHCID 10443194—
CatalystAzobisisobutyronitrileHCID 6547—
SolventCarbon TetrachlorideHCID 5943—
Product1,1'-Biphenyl, 4'-(bromomethyl)-2-nitro-HCID 1177907292.1%

Reaction Steps

A solution/suspension of 3.74 g (17.5 mmol) 2-nitro-4'-methylbiphenyl, 123 mg (0.9 mmol) AIBN, and 3.43 g (19.3 mmol) NBS in 180 mL CCl4 was refluxed for 30 minutes. The mixture was cooled to room temperature, was filtered through a medium fritted funnel, was washed with water, was dried over magnesium sulfate, was stripped of solvent in vacuo, and was chromatographed on silica gel under medium pressure using 7% ethyl acetate in hexanes to give 4.71 g (92% yield) of the title compound as a light yellow crystalline solid. Rf 0.21 in 10% EtOAc/hexane, visualized by UV and ammonium molybdate/ceric sulfate stain.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05250521
Source datasetuspto-grants-1993_10
ORD IDord-c5952f2b9ae747d782b14d29b14f9e3f
Source noteuspto-grants-1993_10