HuagongsheHuagongshe Chemistry Print Report · For research reference only
Azobisisobutyronitrile → 7-(Bromomethyl)-4-phenylquinoline-2-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 7-Methyl-4-phenylquinoline-2-carbonitrile | HCID 57437831 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 7-(Bromomethyl)-4-phenylquinoline-2-carbonitrile | HCID 57437832 | — |
Reaction Steps
A solution of 7-methyl-4-phenylquinoline-2-carbonitrile (11.2 g, 41.7 mmol), N-bromo-succinimide (12.2 g, 68.6 mmol) and AIBN (2,2′-azobisisobutyronitrile) (200 mg) in carbon tetrachloride (200 mL) was heated at reflux overnight. The reaction was cooled to ambient temperature and the solid residue was filtered. The filtrate was concentrated under reduced pressure. The crude product was purified by flash column chromatography (eluting with 5% ethyl acetate in hexane) to give the title compound. 1H NMR (400 MHz, acetone-d6): δ 8.30 (s, 1H), 8.06 (d, 1H), 7.90 (s, 1H), 7.87 (d, 1H), 7.6-7.7 (m, 5H), 4.95 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07960409B2 |
| Source dataset | uspto-grants-2011_06 |
| ORD ID | ord-ad51e95d5f2a4fe887226f09a875a790 |
| Source note | uspto-grants-2011_06 |