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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 353323Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/353323

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzoyl PeroxideHCID 7187—
EduktN-bromobutanimideHCID 67184—
Edukt6-MethylquinoxalineHCID 242567—
Edukt6-(Bromomethyl)quinoxalineHCID 10214510—
LösungsmittelChlorobenzeneHCID 7964—
LösungsmittelPentaneHCID 8003—
LösungsmittelButylamineHCID 8007—
ProduktN-(Quinoxalin-6-ylmethyl)butan-1-amineHCID 12071593—

Reaktionsbedingungen

Temperatur85 °C

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06750343B2
Quelldatensatzuspto-grants-2004_06
ORD IDord-6bd3ee9d2695469e9d5b114ef71ea79d
Quellennotizuspto-grants-2004_06