Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1107Erstellt: 23. Oktober 2026

Methyl Bromide → N-(2-hydroxypropyl)-N,N-dimethyl-N-[3-(12-hydroxyoctadecyl)-2-hydroxypropyl]ammonium bromide

https://huagongshe.com/de/reaction/1107

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl BromideHCID 6323—
Edukt2-(Methylamino)ethanolHCID 8016—
Edukt1-[N-Methyl-N-(2-hydroxyethyl)amino]-3-(12-hydroxyoctadecyl)-2-propanolHCID 19694598—
EduktN-(3-methoxy-2-hydroxy-propyl)-N-methyl-2-hydroxyethylamineHCID 19694612—
Edukt12-Hydroxyoctadecyl glycidyl etherHCID 19694653—
LösungsmittelDiethyl EtherHCID 3283—
ProduktN-(2-hydroxypropyl)-N,N-dimethyl-N-[3-(12-hydroxyoctadecyl)-2-hydroxypropyl]ammonium bromideHCID 1969460390%

Reaktionsschritte

1-[N-Methyl-N-(2-hydroxyethyl)amino]-3-(12-hydroxyoctadecyl)-2-propanol was first prepared from 12-hydroxyoctadecyl glycidyl ether and N-methylethanolamine in the same manner as in the preparation of N-(3-methoxy-2-hydroxy-propyl)-N-methyl-2-hydroxyethylamine in Preparation Example 24. A 200-ml autoclave was charged with 6.3 g (15 mmol) of the thus-prepared compound, 100 ml of diethyl ether and 14.2 g of methyl bromide, and the resultant mixture was stirred at 48° C. for 8 hours. The reaction mixture was then concentrated under reduced pressure, and the resultant residue was dissolved in methanol. Diethyl ether was added to the solution to form crystals. The crystals were collected by filtration, thereby obtaining 6.9 g (yield: 90%) of the title compound (IIb-4).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05723497
Quelldatensatzuspto-grants-1998_03
ORD IDord-540e2d8dfa8f4e3c817851023a8dc240
Quellennotizuspto-grants-1998_03