HuagongsheHuagongshe Chemistry Print Report · For research reference only
Azobisisobutyronitrile → 2-(4-Bromomethylphenyl)4-chlorobenzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 4-Chloro-2-(4-methylphenyl)benzonitrile | HCID 22417997 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 2-(4-Bromomethylphenyl)4-chlorobenzonitrile | HCID 22418000 | — |
Reaction Steps
6.83 g of 4-chloro-2-(4-methylphenyl)benzonitrile, 5.34 g of N-bromosuccinimide and 0.1 g of α,α'-azobis(isobutyronitrile) were heated in 220 ml of carbon tetrachloride under reflux for 2 hr. The succinimide was removed by filtration, and the filtrate was concentrated. The residue was crystallized from a mixed solvent of tetrahydrofuran-isopropyl ether. The yield was 5.6 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05298518 |
| Source dataset | uspto-grants-1994_03 |
| ORD ID | ord-69f01f20e248435cbe1493319125a183 |
| Source note | uspto-grants-1994_03 |