HuagongsheHuagongshe Chemistry Print Report · For research reference only
Azobisisobutyronitrile → HCID 67993023, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 67992953 | HCID 67992953 | — |
| Reactant | HCID 77230840 | HCID 77230840 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | HCID 67993023 | HCID 67993023 | — |
Reaction Steps
A mixture of the intermediate from Step B (0.322 g, 1.903 mmol), NBS (0.373 g, 2.09 mmol), and AIBN (0.016 g, 0.095 mmol) in 15 mL of CCl4 was refluxed for 1 hour. The mixture was cooled to room temperature, filtered, and concentrated. The residue was purified by silica gel chromatography using a hexanes/EtOAc gradient to give a 7:1 mixture of the indicated product and methyl 2-bromo-2-[4-(bromomethyl)-1,3-oxazol-2-yl]propanoate (pale yellow oil). The mixture was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09365574B2 |
| Source dataset | uspto-grants-2016_06 |
| ORD ID | ord-9c304fd6eed14f4baf35a91c4aadb382 |
| Source note | uspto-grants-2016_06 |