Reaktionsgleichung
[Cl-:1].[CH:2]([N:4]([CH2:9][CH2:10][CH2:11][N+:12]([CH3:15])([CH3:14])[CH3:13])[CH2:5][CH2:6][CH2:7][OH:8])=O.C=O>C(O)=O>[ClH:1].[Cl-:1].[OH:8][CH2:7][CH2:6][CH2:5][N:4]([CH2:9][CH2:10][CH2:11][N+:12]([CH3:15])([CH3:14])[CH3:13])[CH3:2]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A mixture of 2 g. of 3-[N'-formyl-N'-(3-hydroxypropyl)amino]-N,N,N-trimethyl-1-propanaminium chloride 4 g. of 99% formic acid and 2 ml. of formalin is stirred and heated at 100° for 17 hours. To the cooled mixture is added 11 ml. of concentrated hydrochloric acid and the reaction mixture is concentrated under reduced pressure. The product is taken up in 35 ml. of 1 N hydrochloric acid and the solution is filtered and concentrated to dryness under reduced pressure yielding 3-[N'-(3-hydroxypropyl)-N'-methylamino]-N,N,N-trimethyl-1-propanaminium chloride hydrochloride.
Aufarbeitung
- additionA mixture of 2 g
- temperatureheated at 100° for 17 hours
- additionTo the cooled mixture is added 11 ml
- concentrationof concentrated hydrochloric acid and the reaction mixture is concentrated under reduced pressure
- filtrationof 1 N hydrochloric acid and the solution is filtered
- concentrationconcentrated to dryness under reduced pressure
Quellen und Nachweise
- ORD-Eintrag
- ord-d9d42b07a44148eda82f8ac09fe1cb9a
- Quelldatensatz
- uspto-grants-1977_04
- Patentnummer
- US04016209
Verknüpfte Notizen
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