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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1255562Generated: October 31, 2026

Benzoyl Peroxide → 6-(Bromomethyl)quinoxaline

https://huagongshe.com/reaction/1255562

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 numberUS08461156B2
Source datasetuspto-grants-2013_06
ORD IDord-9a59fb2be208480d91a6a3b887c8b0d1
Source noteuspto-grants-2013_06