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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5238Generated: October 29, 2026

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

https://huagongshe.com/reaction/5238

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 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 numberUS05243054
Source datasetuspto-grants-1993_09
ORD IDord-38557339d9a449aeba84ca978a2ba6b2
Source noteuspto-grants-1993_09