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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 353314Erstellt: 24. Oktober 2026

Ethyl Bromide → 9-((N-(5-hydroxypentyl)-N-(ethyl)amino)methyl)anthracene

https://huagongshe.com/de/reaction/353314

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl BromideHCID 6332—
EduktPotassium CarbonateHCID 11430—
Edukt9-((5-Hydroxypentyl)aminomethyl)anthraceneHCID 10880907—
LösungsmittelAcetonitrileHCID 6342—
Produkt9-((N-(5-hydroxypentyl)-N-(ethyl)amino)methyl)anthraceneHCID 2266220198%

Reaktionsschritte

9-((5-hydroxypentyl)aminomethyl)anthracene (1.00 g, 3.41 mol) and K2CO3 (0.518 g, 3.75 mmol) were taken up in 25 mL acetonitrile. Ethyl bromide (11.14 g, 102 mmol) was added and the mixture was refluxed under nitrogen for 24 h. The mixture was filtered on a sintered-glass frit and the solvent and excess ethyl bromide was removed under reduced pressure. Removal of the solvent afforded 1.07 g (98% yield) of 6 as a yellow solid; 1H NMR (300.13 MHz, CD3CN) δ1.15 (m, 2H), 1.38 (m, 5H), 1.81 (m, 2H), 3.05 (m, 4H), 3.49 (t, 2H), 5.21 (s, 2H), 7.45 (m, 2H), 7.62 (m, 2H), 8.05 (d, 2H), 8.44 (m, 3H); 13C-{1H} NMR (75.4 MHz, CDCl3) δ131.8, 131.3, 130.8, 129.6, 128.0, 125.6, 124.0, 61.7, 53.1, 49.4, 48.7, 31.4, 23.9, 23.3, 10.0.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06750311B1
Quelldatensatzuspto-grants-2004_06
ORD IDord-8ebc8f79b373446f9d171657094efa16
Quellennotizuspto-grants-2004_06