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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 530382Generated: November 4, 2026

Azobisisobutyronitrile → 3-(Bromomethyl)-5-nitrobiphenyl

https://huagongshe.com/reaction/530382

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
Reactant3-Methyl-5-nitrobiphenylHCID 53652407—
SolventCarbon TetrachlorideHCID 5943—
Product3-(Bromomethyl)-5-nitrobiphenylHCID 90042276—

Reaction Conditions

Temperature80 °C

Reaction Steps

NBS (184 mg, 1.032 mmol) and AIBN (15.4 mg, 0.04 mmol) were added to a solution of 3-methyl-5-nitrobiphenyl (200 mg, 0.938 mmol) in carbon tetrachloride (1.88 mL) and then the reaction mixture was heated to 80° C. for 3 hours. Additional AIBN (15.4 mg, 0.04 mmol) was added to the reaction mixture and was heated for additional 1 hour. The mixture was purified directly by silica gel column chromatography (ethyl acetate/hexanes) to yield 3-(bromomethyl)-5-nitrobiphenyl.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09353066B2
Source datasetuspto-grants-2016_05
ORD IDord-97a6d1d6e25a47d7863e2d53a1d0c996
Source noteuspto-grants-2016_05