CH196872A - Process for the preparation of a quaternary aminoacetic acid amide derivative. - Google Patents
Process for the preparation of a quaternary aminoacetic acid amide derivative.Info
- Publication number
- CH196872A CH196872A CH196872DA CH196872A CH 196872 A CH196872 A CH 196872A CH 196872D A CH196872D A CH 196872DA CH 196872 A CH196872 A CH 196872A
- Authority
- CH
- Switzerland
- Prior art keywords
- quaternary
- preparation
- acid amide
- amide derivative
- aminoacetic acid
- Prior art date
Links
Landscapes
- Coloring (AREA)
Description
Verfahren zur Darstellung eines quaternären Aminoessigsäureamidderivates. Es wurde gefunden, dass man durch Um setzung von Chloracetyl-N-spermacetanilid, wie es aus N-Spermacetanilirr, hergestellt unter Verwendung der Mischung der gesättigten und ungesättigten Spermacetalkohole, die durch Verseifung von Spermacetöl erhalten werden, und Chloracetylchlorid erhältlich ist,
mit Trimethylamin zum quaternären Dimethyl- aminoessigsäu re -N- spermacetanilid- Chlorme- thylat gelangen kann. Die neue Verbindung, in festem Zustand eine salben- bis wachs artige Masse von brauner Farbe, löst sich sehr leicht in Wasser und weist stark aus geprägte, kapillaraktive Eigenschaften auf.
Sie soll Verwendung finden als Weich- machungsmittel, Abziehmittel für Naphthol- AS- und güpenfärbungen und als Mittel zum Verbessern der Wasserechtheit von direkt gefärbter, nativer und umgefällter Zellulose.
<I>Beispiel:</I> 37 g Chloracefyl-N-spermacetanilid werden mit 37 g Trimethylamin, verwendet als 33 /o- ige, alkoholische Lösung, mit 200 g Äthyl- alkohol b Stunden im Autoklav auf 130 bis 140' erhitzt; dann werden Alkohol und über schüssiges Trimethylamin abdestilliert und der Rückstand kurze Zeit im Vakuum ge trocknet. Man erhält eine braune, wachs ähnliche, in Wasser klar lösliche Masse, die stark ausgeprägte, kapillaraktiveEigenschaften aufweist.
Die neue Verbindung soll Verwen dung finden als Weichmachungsmittel, Abzieh mittel für Naphthol-AS- und güpenfärbungen und als Mittel zum Verbessern der Wasser echtheit von direkt gefärbter, nativer und um gefällter Zellulose.
Process for the preparation of a quaternary aminoacetic acid amide derivative. It has been found that by converting chloroacetyl-N-spermacetanilide, as it is produced from N-spermacetanilirr, using the mixture of the saturated and unsaturated spermacetal alcohols obtained by saponification of spermacetol and chloroacetyl chloride,
with trimethylamine, the quaternary dimethylaminoacetic acid -N- spermacetanilide chloromethylate can be obtained. The new compound, in the solid state an ointment-like to waxy mass of brown color, dissolves very easily in water and has strong, capillary-active properties.
It is said to be used as a plasticizer, a stripping agent for naphthol, AS and güpen dyeings and as an agent for improving the waterfastness of directly dyed, native and reprecipitated cellulose.
<I> Example: </I> 37 g of chloracefyl-N-spermacetanilide are heated with 37 g of trimethylamine, used as a 33% alcoholic solution, with 200 g of ethyl alcohol for b hours in the autoclave to 130 to 140 °; then alcohol and excess trimethylamine are distilled off and the residue is dried in vacuo for a short time. A brown, wax-like mass is obtained which is clearly soluble in water and which has very pronounced, capillary-active properties.
The new compound is said to be used as a plasticizer, a stripping agent for naphthol AS and güpenfyeing and as a means to improve the water fastness of directly dyed, native and reprecipitated cellulose.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE196872X | 1935-12-23 | ||
DE198052X | 1935-12-23 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH196872A true CH196872A (en) | 1938-03-31 |
Family
ID=25758378
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH196872D CH196872A (en) | 1935-12-23 | 1936-11-12 | Process for the preparation of a quaternary aminoacetic acid amide derivative. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH196872A (en) |
-
1936
- 1936-11-12 CH CH196872D patent/CH196872A/en unknown
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