HuagongsheHuagongshe Chemistry Print Report · For research reference only
Azobisisobutyronitrile → 4'-(Bromomethyl)-[1,1'-biphenyl]-2-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2-(p-Tolyl)benzamide | HCID 10171345 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 4'-(Bromomethyl)-[1,1'-biphenyl]-2-carboxamide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05243054 |
| Source dataset | uspto-grants-1993_09 |
| ORD ID | ord-38557339d9a449aeba84ca978a2ba6b2 |
| Source note | uspto-grants-1993_09 |