HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 4-Quinolinecarboxylic acid, 3-(bromomethyl)-2-phenyl-, methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Methyl 3-methyl-2-phenylquinoline-4-carboxylate | HCID 230804 | — |
| Catalyst | Benzoyl Peroxide | HCID 7187 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-Quinolinecarboxylic acid, 3-(bromomethyl)-2-phenyl-, methyl ester | HCID 10498448 | 203.5% |
Reaction Steps
10 g (36 mmol) of 3-methyl-2-phenyl-quinoline-4-carboxylic acid methyl ester (compound of Description 1) were dissolved in 500 ml of CH3CN; 13 g (72 mmol) of N-bromosuccinimide were added and the reaction mixture was heated to reflux. After adding 1 g (4.1 mmol) of dibenzoylperoxide; the reaction was refluxed for 24 h; then additional 4 g (22.5 mmol) of N-bromosuccinimide and 0.5 g (2.0 mmol) of dibenzoylperoxide were added and the reaction was refluxed for 4 h. The solvent was evaporated in vacuo to dryness to yield 26.1 g of crude title compound which has been used in the following reaction without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06613770B1 |
| Source dataset | uspto-grants-2003_09 |
| ORD ID | ord-42d57b0ffbb849c79be5df80268183d4 |
| Source note | uspto-grants-2003_09 |