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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 353323Generated: October 25, 2026

Benzoyl Peroxide → N-(Quinoxalin-6-ylmethyl)butan-1-amine

https://huagongshe.com/reaction/353323

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
Reactant6-MethylquinoxalineHCID 242567—
Reactant6-(Bromomethyl)quinoxalineHCID 10214510—
SolventChlorobenzeneHCID 7964—
SolventPentaneHCID 8003—
SolventButylamineHCID 8007—
ProductN-(Quinoxalin-6-ylmethyl)butan-1-amineHCID 12071593—

Reaction Conditions

Temperature85 °C

Reaction Steps

In a 50 ml flask, 6-methyl-quinoxaline (1.25 g, 8.68 mmol) was dissolved together with N-bromosuccinimide (2.32 g, 13.0 mmol) and benzoyl-peroxide (0.15 g, 0.62 mmol) in 31. g of chlorobenzene. The solution was stirred with heating at 85° C. for 2.0 hours to yield a reddish solution. The solution was cooled down to room temperature and one volume of pentane was added to facilitate the removal of succinimides. The precipitate was washed with pentane and the extracts were combined with the chlorobenzene solution. The yellow solution was vacuum dried to give a yellow residue mainly composed of 6-bromomethyl-quinoxaline. The yellow solid was dissolved in 19.0 g of n-butylamine to give a yellow solution that was stirred at room temperature for ˜5 minutes. Analysis of a sample showed that the 6-bromomethyl-quinoxaline was consumed to give exclusively 6-n-butylaminomethyl-quinoxaline as a deep yellow oil (1.71 g, 92% over all yield). MS (70 ev): 215 M+, 172 (M+—CH3—CH2—CH2),143 (M+—CH3—CH2—CH2—CH2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06750343B2
Source datasetuspto-grants-2004_06
ORD IDord-6bd3ee9d2695469e9d5b114ef71ea79d
Source noteuspto-grants-2004_06