HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1471761Generated: November 1, 2026
Azobisisobutyronitrile → 6-(Bromomethyl)pyridine-3-carbonitrile
https://huagongshe.com/reaction/1471761
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 6-Methylpyridine-3-carbonitrile | HCID 281995 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 6-(Bromomethyl)pyridine-3-carbonitrile | HCID 21927776 | 37.5% |
Reaction Steps
Into a 250-mL round-bottom flask, was placed a solution of 6-methylpyridine-3-carbonitrile (8 g, 67.72 mmol, 1.00 equiv) in CCl4 (125 mL). N-Bromosuccinimide (13.4 g, 75.29 mmol, 1.10 equiv), and AIBN (480 mg, 2.92 mmol, 0.04 equiv) were added to the reaction solution. The resulting solution was stirred for 5 h at 85° C. The resulting mixture was concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1:5) as eluent to yield 5 g (37%) of 6-(bromomethyl)pyridine-3-carbonitrile as a beige solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09012450B2 |
|---|
| Source dataset | uspto-grants-2015_04 |
|---|
| ORD ID | ord-bf24625a23ea48dbb7471a90ec8a2e6e |
|---|
| Source note | uspto-grants-2015_04 |
|---|