HuagongsheHuagongshe Chemistry Print Report · For research reference only
Azobisisobutyronitrile → 4-Bromomethyl-2-trifluoromethylbenzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 4-Methyl-2-(trifluoromethyl)benzonitrile | HCID 2775597 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 4-Bromomethyl-2-trifluoromethylbenzonitrile | HCID 59164585 | 157.1% |
Reaction Steps
To a refluxing mixture of 5.0 g 4-Methyl-2-(trifluoromethyl)benzonitrile in 50 ml tetrachloromethane were added a mixture of 5.77 g N-bromosuccinimide and 1.77 g 2,2′-azobis(2-methylpropionitrile). The reaction mixture was heated under reflux for three hours. The reaction mixture was filtered through a pad of celite and the solvent was removed in vacuo to obtain 11.2 g crude 4-Bromomethyl-2-trifluoromethyl-benzonitrile (impurified with the dibromo product) as a white solid. This material was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07655679B2 |
| Source dataset | uspto-grants-2010_02 |
| ORD ID | ord-f1dbe9fd966e46c483507ca4ba370b6e |
| Source note | uspto-grants-2010_02 |