HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl Peroxide → 6-(Bromomethyl)quinoxaline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl Peroxide | HCID 7187 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 6-Methylquinoxaline | HCID 242567 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 6-(Bromomethyl)quinoxaline | HCID 10214510 | 77.5% |
Reaction Steps
To a solution of 6-methylquinoxaline (10.0 g, 69.4 mmol) in CCl4 (80 mL) was added NBS (13.5 g, 76.3 mmol) and benzoyl peroxide (BP, 1.7 g, 6.9 mmol) at room temperature. The mixture was heated at reflux for 2 hours. After cooling, the mixture was evaporated under vacuum to give a yellow solid, which was extracted with Petroleum Ether (50 mL×5). The extracts were concentrated under vacuum. The organics were combined and concentrated to give crude 6-bromomethylquinoxaline (12.0 g), which was used directly in the next step. 1H NMR (300 MHz, CDCl3) δ 8.85-8.87 (m, 2H), 8.10-8.13 (m, 2H), 7.82 (dd, J=2.1, 8.7 Hz, 1H), 4.70 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07741321B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-dbdee4d6eed2475087add1eab84006da |
| Source note | uspto-grants-2010_06 |