CH179660A - Process for the preparation of a benzimidazolium derivative. - Google Patents
Process for the preparation of a benzimidazolium derivative.Info
- Publication number
- CH179660A CH179660A CH179660DA CH179660A CH 179660 A CH179660 A CH 179660A CH 179660D A CH179660D A CH 179660DA CH 179660 A CH179660 A CH 179660A
- Authority
- CH
- Switzerland
- Prior art keywords
- benzimidazolium
- ethyl
- derivative
- preparation
- methyl
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/06—Benzimidazoles; Hydrogenated benzimidazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 2
- C07D235/08—Radicals containing only hydrogen and carbon atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Description
Verfahren zur Herstellung eines Benzimidazoliumderivates. Es wurde gefunden, dass man in einfacher Weise das ,u-Heptadecenyl-N'-methyl-N- äthyl-benzimidazoliumchlorid erhalten kann, wenn man auf das mit Hilfe der Ölsäure erhältliche A-Heptadecenyl-N-äthyl-benzimid- azolchlorhydrat Methylalkohol einwirken lässt. Das ,u-Heptadeeenyl-N'-methyl-N-äthyl- benzimidazoliumchlorid bildet eine sich fettig anfühlende, helle Masse, deren wässerige Lö sungen stark kapillaraktiv sind.
Beispiel: Man erhitzt während etwa 10 Stunden 40 Teile ,u-Hepta.decenyl-N-äthyl-benzimid- azolchlorhydrat mit 6 Teilen Methylalkohol im geschlossenen Gefäss auf 170 bis 175 . Nach .dem Erkalten erhält man das ,u-Hepta- decenyl - N'-methyl-N-äthyl-benzimida.zolium- A.hIorid in Form eins halbfesten Produktes, >da gegebenenfalls mit Benzin gereinigt wer- den kann und das in Wasser klar und schäu mend löslich ist.
Das ss-Heptadecenyl-N'- methyl-N-äthyl-benzimidazoliumchlorid kann als Hilfsstoff in der Textilindustrie verwen det werden.
Process for the preparation of a benzimidazolium derivative. It has been found that u-heptadecenyl-N'-methyl-N-ethylbenzimidazolium chloride can be obtained in a simple manner if methyl alcohol is used to act on the A-heptadecenyl-N-ethylbenzimidazole chlorohydrate obtainable with the aid of oleic acid leaves. The, u-heptadeeenyl-N'-methyl-N-ethyl benzimidazolium chloride forms a greasy, light-colored mass, the aqueous solutions of which are highly capillary.
Example: 40 parts of u-hepta.decenyl-N-ethylbenzimidazole chlorohydrate with 6 parts of methyl alcohol are heated to 170 to 175 in a closed vessel for about 10 hours. After cooling, the u-heptadecenyl-N'-methyl-N-ethyl-benzimida.zolium-chloride is obtained in the form of a semi-solid product, since it can be cleaned with gasoline if necessary and that in water is clear and foamingly soluble.
The ss-heptadecenyl-N'-methyl-N-ethyl-benzimidazolium chloride can be used as an auxiliary in the textile industry.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH179660T | 1934-02-01 | ||
CH175026T | 1934-02-01 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH179660A true CH179660A (en) | 1935-09-15 |
Family
ID=25719587
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH179660D CH179660A (en) | 1934-02-01 | 1934-02-01 | Process for the preparation of a benzimidazolium derivative. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH179660A (en) |
-
1934
- 1934-02-01 CH CH179660D patent/CH179660A/en unknown
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