HuagongsheHuagongshe Chemistry Print Report · For research reference only
Azobisisobutyronitrile → 3,5-Dibromo-2-(bromomethyl)pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 3,5-Dibromo-2-methylpyridine | HCID 619705 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 3,5-Dibromo-2-(bromomethyl)pyridine | HCID 53417177 | 55% |
Reaction Steps
To a solution of 52A (1.25 g, 4.98 mmol) in CCl4 (7 ML) was added NBS (0.89 g, 4.98 mmol) followed by catalytic AIBN and the mixture was heated to reflux for 4 hours. The reaction was cooled to room temperature, filtered and concentrated in vacuo. The residue was purified by flash chromatography (SiO2, 10% CH2Cl2/Hexane then 50% CH2Cl2/Hexane) to give 52B (0.90 g, 55%). HPLC Rt=2.85 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07378426B2 |
| Source dataset | uspto-grants-2008_05 |
| ORD ID | ord-989c30392564450eb7b6d497f16e4150 |
| Source note | uspto-grants-2008_05 |