HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2306227Generated: November 3, 2026
Azobisisobutyronitrile → HCID 18536041, compound
https://huagongshe.com/reaction/2306227
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 18536178 | HCID 18536178 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | HCID 18536041 | HCID 18536041 | — |
Reaction Steps
A mixture of methanesulfonic acid 4-bromo-3-methylphenyl ester, as described above in Step B, (14.3 g, 53.9 mmol), N-bromosuccinimide (14.4 g, 80.9 mmol), and 2,2′-azobisisobutyronitrile (1.34 g, 8.16 mmol) in CCl4 was heated at 80° C. for 18 hours. The solvent was removed under reduced pressure and the residue was purified by silica gel chromatography, eluting with a gradient of hexane—5% to 20% EtOAc, to yield the titled product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06441017B1 |
|---|
| Source dataset | uspto-grants-2002_08 |
|---|
| ORD ID | ord-31c3f441d8e84cf4bf2ed2b4e671501e |
|---|
| Source note | uspto-grants-2002_08 |
|---|