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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1505103Generated: November 1, 2026

Benzoyl Peroxide → 6-(Bromomethyl)quinoxaline

https://huagongshe.com/reaction/1505103

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
Reactant6-MethylquinoxalineHCID 242567—
SolventCarbon TetrachlorideHCID 5943—
Product6-(Bromomethyl)quinoxalineHCID 1021451077.5%

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, 2 H), 8.10-8.13 (m, 2H), 7.82 (dd, J=2.1, 8.7 Hz, 1 H), 4.70 (s, 2 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216969B2
Source datasetuspto-grants-2015_12
ORD IDord-4f2703cf038d4059bca169cfbc7f8520
Source noteuspto-grants-2015_12