Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 263811Erstellt: 25. Oktober 2026

4-(3,3,3-Triphenylpropoxy)benzyl chloride → N,N,N-Trimethyl-[4-(3,3,3-triphenylpropoxy)phenyl]methylammonium chloride

https://huagongshe.com/reaction/263811

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-(3,3,3-Triphenylpropoxy)benzyl chlorideHCID 54438256—
EduktTrimethylamine ethanolHCID 86589564—
ProduktN,N,N-Trimethyl-[4-(3,3,3-triphenylpropoxy)phenyl]methylammonium chlorideHCID 86751025—

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

A suspension of 4-(3,3,3-triphenylpropoxy)benzyl chloride, prepared in example 28, (413 mg, 1.0 mmol) in commercial 33% trimethylamine-ethanol solution was sealed in a screw-topped culture tube and was heated to 80° C. for 24 hr. The mixture was cooled and the solvent evaporated, and the residue recrystallized from isopropanolethyl acetate to provide the title compound as a hydrate, a white powder, mp 224°-225° C. (dec). 1H NMR (CDCl3) δ 7.43 (d, J=8.7 Hz, 2H) 7.15-7.35 (m, 15H), 6.71 (d, J=8.7 Hz, 2H), 4.82 (s, 2H), 3.73 (t, J=7.7 Hz, 2H), 3.31 (s, 9H), 3.13 (t, J=7.7 Hz, 2H). Anal. calcd. for C31H34NO.Cl.1.5H2O: C, 74.60; H, 7.47; N, 2.81; Cl, 7.10. Found: C, 74.99; H, 7.49; N, 2.83; Cl, 7.07.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05643950
Quelldatensatzuspto-grants-1997_07
ORD IDord-0fdbdc79936b4fccb41f7a4e058ddd3e
Quellennotizuspto-grants-1997_07