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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 397227Erstellt: 23. Oktober 2026

Hepta-1,6-dien-4-amine → N-(N,N-Dimethyl-N-dodecylammonio)butyldiallylmethylammonium Chloride Bromide

https://huagongshe.com/de/reaction/397227

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHepta-1,6-dien-4-amineHCID 12791689—
Edukt4-Chlorobutyldimethyldodecylammonium bromideHCID 15870133—
LösungsmittelMethanolHCID 887—
ProduktN-(N,N-Dimethyl-N-dodecylammonio)butyldiallylmethylammonium Chloride BromideHCID 8659380367,2%

Reaktionsbedingungen

Temperatur65 °C

Reaktionsschritte

A mixture of 22 g diallylmethylamine and 75 g 4-chlorobutyldimethyldodecyl-ammonium bromide were dissolved in 100 mL methanol and the reaction mixture was stirred at 65° C. for 48 hours. The progress of the reaction was monitored by the disappearance of the diallylmethylamine by thin layer chromatography (TLC). After cooling to room temperature, the solvent was removed under reduced pressure. The residual viscous oil was precipitated into 800 mL dry ether with rapid stirring. The ether layer was decanted and the residue was again treated with 500 mL dry ether. After stirring for 15 minutes the solvent was removed and the oily residue was dried under vacuum at 35° C. for 48 hours, yielding 65 g of the product.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06610283B1
Quelldatensatzuspto-grants-2003_08
ORD IDord-ca68ff58234a4e23b8c52b21d7ba058e
Quellennotizuspto-grants-2003_08