CH177817A - Process for the preparation of an imidazole derivative. - Google Patents
Process for the preparation of an imidazole derivative.Info
- Publication number
- CH177817A CH177817A CH177817DA CH177817A CH 177817 A CH177817 A CH 177817A CH 177817D A CH177817D A CH 177817DA CH 177817 A CH177817 A CH 177817A
- Authority
- CH
- Switzerland
- Prior art keywords
- imidazole derivative
- preparation
- benzimidazole
- water
- hydrochloride
- 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)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Description
*Verfahren zur Herstellung eines Imidazolderivates. Es wurde gefunden, dass man ein neues Imidazolderivat erhält, wenn man Benzimi- dazol mit einem Ester des Laurylalkohols behandelt. Das neue Imidazolderivat verbin det sich mit Mineralsäure zu Salzen, z. B.
mit Salzsäure zum N-Lauryl-berizimidazol- hydrochlorid, das mit Wasser stark scbäu- mende Lösungen gibt und ein ausgezeich netes Weichmachungsmittel für Tiskose- kunstseide darstellt. <I>Beispiel</I> 49 Teile Benzimidazol werden mit 80 Teilen Laurylchlorid während etwa 8 Stun den bei<B>1600</B> gerührt.
Sobald eine Probe der Reaktionsmasse sich in angesäuertem Wasser klar löst, unterbricht man das weitere Er hitzen, wobei nach dem Erkalten das Reak- tionsprodukt als eine talgige Masse erhalten wird, die nötigenfalls durch Aufnahme in Alkohol und Entfärben mit Tierkohle völlig entfärbt werden kann.
* Process for the production of an imidazole derivative. It has been found that a new imidazole derivative is obtained if benzimidazole is treated with an ester of lauryl alcohol. The new imidazole derivative connects with mineral acid to form salts such. B.
with hydrochloric acid to form N-lauryl-berizimidazole hydrochloride, which gives strong foaming solutions with water and is an excellent softening agent for artificial silk. <I> Example </I> 49 parts of benzimidazole are stirred with 80 parts of lauryl chloride for about 8 hours at <B> 1600 </B>.
As soon as a sample of the reaction mass dissolves clearly in acidified water, further heating is interrupted, whereby after cooling the reaction product is obtained as a tallowy mass which, if necessary, can be completely decolorized by absorption in alcohol and decolorization with animal charcoal.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH175673T | 1933-12-15 | ||
CH177817T | 1933-12-15 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH177817A true CH177817A (en) | 1935-06-15 |
Family
ID=25719719
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH177817D CH177817A (en) | 1933-12-15 | 1933-12-15 | Process for the preparation of an imidazole derivative. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH177817A (en) |
-
1933
- 1933-12-15 CH CH177817D patent/CH177817A/en unknown
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