Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 350822Erstellt: 26. Oktober 2026

Phenethylamine → 8-(N-Benzyl-N-methylamino)octan-1-ol

https://huagongshe.com/reaction/350822

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhenethylamineHCID 1001—
EduktSodium IodideHCID 5238—
EduktAcetonitrileHCID 6342—
EduktSodium CarbonateHCID 10340—
Edukt1-Octanol, 8-chloro-HCID 90012—
Lösungsmitteltert-Butyl methyl etherHCID 15413—
Produkt8-(N-Benzyl-N-methylamino)octan-1-olHCID 1666215396%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

From 8-Chlorooctan-1-ol: A 2-L flask was charged with benzylmethylamine (270 g, 2.23 mol), sodium carbonate (157 g, 1.48 mol), sodium iodide (11.1 g, 0.074 mol), 8-chlorooctanol (122 g, 0.74 mol) and acetonitrile (1000 mL) and the resulting suspension was stirred at 80° C. for 20–30 h. The reaction mixture was then concentrated to a volume of about 500 mL and water (600 mL) and tert-butyl methyl ether (1000 mL) were added. The MTBE layer was then separated and washed with water (500 mL). The MTBE solution was concentrated by distillation under vacuum to provide an oil and the oil was then further concentrated by distillation under high vacuum to remove excess benzylmethylamine. N-methyl-2-pyrrolidone (300 mL) was then added to the remaining oil and this solution concentrated by distillation under high vacuum to provide an oil. The oil was dissolved in MTBE (1000 mL) and the resulting solution was washed with water (2×500 mL), brine (500 mL), dried with sodium sulfate (100 g), filtered and concentrated by distillation to afford the title compound as an oil (178 g, 96% yield, >95% purity).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07183292B2
Quelldatensatzuspto-grants-2007_02
ORD IDord-2396a5983d5a474c8730bd84baf2517b
Quellennotizuspto-grants-2007_02