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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 17931Erstellt: 26. Oktober 2026

Benzoyl Peroxide → 6-(Bromomethyl)quinoxaline

https://huagongshe.com/reaction/17931

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzoyl PeroxideHCID 7187—
EduktN-bromobutanimideHCID 67184—
Edukt6-MethylquinoxalineHCID 242567—
LösungsmittelCarbon TetrachlorideHCID 5943—
Produkt6-(Bromomethyl)quinoxalineHCID 1021451077,5%

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07741321B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-dbdee4d6eed2475087add1eab84006da
Quellennotizuspto-grants-2010_06