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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1870927Generated: October 31, 2026

Azobisisobutyronitrile → 4'-(Bromomethyl)-[1,1'-biphenyl]-2-carboxamide

https://huagongshe.com/reaction/1870927

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
Reactant2-(p-Tolyl)benzamideHCID 10171345—
SolventBenzeneHCID 241—
Product4'-(Bromomethyl)-[1,1'-biphenyl]-2-carboxamideHCID 15219006—

Reaction Conditions

Temperature65 °C

Reaction Steps

A mixture of 4'-methylbiphenyl-2-carboxamide (2.1 g), N-bromo-succinimide (2.5 g) and azobisisobutyronitrate (AIBN; 82 mg) in benzene (20 ml) was stirred for 20 hours at 60 to 70° C. Resulting crystalline precipitates were collected by filtration, washed with isopropylether and suspended in water. The suspension was stirred for 30 minutes, and insoluble materials were collected by filtration and dried to give crude crystals. Recrystallization from ethyl acetate-methanol afforded colorless needles (1.6 g, 55%), m.p. 220-221° C.(decomp.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06100252
Source datasetuspto-grants-2000_08
ORD IDord-d101f7e84ad64eeca95fe1b261990935
Source noteuspto-grants-2000_08