CH205062A - Process for the preparation of a quaternary nitrogen compound. - Google Patents
Process for the preparation of a quaternary nitrogen compound.Info
- Publication number
- CH205062A CH205062A CH205062DA CH205062A CH 205062 A CH205062 A CH 205062A CH 205062D A CH205062D A CH 205062DA CH 205062 A CH205062 A CH 205062A
- Authority
- CH
- Switzerland
- Prior art keywords
- nitrogen compound
- quaternary nitrogen
- preparation
- dimethylethylene diamine
- warm water
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/04—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D233/06—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to ring carbon atoms
- C07D233/08—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to ring carbon atoms with alkyl radicals, containing more than four carbon atoms, directly attached to ring carbon atoms
- C07D233/10—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to ring carbon atoms with alkyl radicals, containing more than four carbon atoms, directly attached to ring carbon atoms with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to ring nitrogen atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Herstellung einer quaternären Stickstoffverbindung. Es wurde gefunden, dass man 1,3-Dimethyl- 2-heptadecylimidazoliniumchlorid erhält, wenn man Stearinsäure mit einem Gemisch, be stehend aus '/2 Mol. N. N'-Dimethyläthylen- diamin und '/2 Mol. N. N'-Dimethyläthyleri- diamindihydrochlorid bei 200 bis<B>2500</B> C um setzt.
Das gebildete Produkt stellt eine Masse dar, die sich in warmem Wasser leicht zu einer in der gälte gelierenden .Flüssigkeit löst; es soll als Textilhilfsmittel verwendet werden. <I>Beispiel:</I> 2,9 g Stearinsäure, 0,9 g N. N'-Dimethyl- äthylendiamin, 1,6 g N. N'-Dimethyläthylen- diamindihydrochlorid werden in einem Kölb- chen erhitzt.
Man steigert unter Rühren innerhalb etwa 5 .Minuten die Temperatur auf 2000 C, innerhalb weiterer 10 Minuten auf 230' C und hält nunmehr zwischen 240 bis 2450 C, bis sich nach einigen Minuten eine Probe in warmem Wasser gut löst und auf Ammoniakzusatz unverändert bleibt.
Das gebildete 1,3-Dimethyl-2-heptadecyl- irnidazoliniumohlorid stellt eine leicht ge- färbte Masse dar, die sich in warmem Wasser leicht zu einer in der gälte gelierenden Flüssigkeit:. lost; es soll als Textilhilfsmittel verwendet werden.
Process for the preparation of a quaternary nitrogen compound. It has been found that 1,3-dimethyl-2-heptadecylimidazolinium chloride is obtained when stearic acid is obtained with a mixture consisting of '/ 2 mol. N. N'-dimethylethylene diamine and' / 2 mol. N. N ' -Dimethyläthyleri- diaminedihydrochloride at 200 to <B> 2500 </B> C.
The product formed is a mass that easily dissolves in warm water to form a liquid that gels in the cold; it is intended to be used as a textile auxiliary. <I> Example: </I> 2.9 g of stearic acid, 0.9 g of N. N'-dimethylethylenediamine, 1.6 g of N. N'-dimethylethylenediamine dihydrochloride are heated in a small flask.
The temperature is increased to 2000 ° C. within about 5 minutes, with stirring, to 230 ° C. within a further 10 minutes and is now kept between 240 to 2450 ° C. until a sample dissolves well in warm water after a few minutes and remains unchanged when ammonia is added.
The 1,3-dimethyl-2-heptadecyl-imidazolinium chloride formed is a lightly colored mass which, in warm water, easily turns into a liquid that gels in the cold. lost; it is intended to be used as a textile auxiliary.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AT205062X | 1936-07-29 | ||
CH200980T | 1937-07-28 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH205062A true CH205062A (en) | 1939-05-31 |
Family
ID=25607752
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH205062D CH205062A (en) | 1936-07-29 | 1937-07-28 | Process for the preparation of a quaternary nitrogen compound. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH205062A (en) |
-
1937
- 1937-07-28 CH CH205062D patent/CH205062A/en unknown
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