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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 17931Generated: October 25, 2026

Benzoyl Peroxide → 6-(Bromomethyl)quinoxaline

https://huagongshe.com/reaction/17931

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

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741321B2
Source datasetuspto-grants-2010_06
ORD IDord-dbdee4d6eed2475087add1eab84006da
Source noteuspto-grants-2010_06