HuagongsheHuagongshe Chemistry Print Report · For research reference only
Azobisisobutyronitrile → HCID 67236432, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | Thiophenol | HCID 7969 | — |
| Reactant | 4-Vinylbenzoic acid | HCID 14098 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 67236432 | HCID 67236432 | 85% |
Reaction Steps
According to the published procedure (Gareau et al., Tet. Lett., 1994, 1837), under nitrogen atmosphere in a 50 mL round bottomed flask containing 4-vinyl-benzoic acid (1.0 g, 6.75 mmoles) in 10 mL of benzene (0.7 M) was added benzenethiol (797 μL, 7.76 mmoles) followed by VAZO™ (Aldrich Chemical Company, 495 mg, 2.02 mmoles). The mixture was stirred for 12 hours at reflux. The resulting solution was cooled at room temperature and the solvent was evaporated under vacuo. The solid was purified by trituration using hexane and dichloromethane to afford 1.94 g (85%) of white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | USRE039850E1 |
| Source dataset | uspto-grants-2007_09 |
| ORD ID | ord-19f4f08e7fe94b8ab815e966b617914f |
| Source note | uspto-grants-2007_09 |