CH164736A - Process for the preparation of a new sulfonic acid. - Google Patents
Process for the preparation of a new sulfonic acid.Info
- Publication number
- CH164736A CH164736A CH164736DA CH164736A CH 164736 A CH164736 A CH 164736A CH 164736D A CH164736D A CH 164736DA CH 164736 A CH164736 A CH 164736A
- Authority
- CH
- Switzerland
- Prior art keywords
- sulfonic acid
- new
- preparation
- mixture
- new sulfonic
- 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)
- Detergent Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Herstellung einer neuen Sulfonsäure. Es wurde gefunden, dass man eine neue Sulfonsäure erhält, wenn man das Imidazol- gemisch, das entsteht durch Kondensieren von o-Phenylendiamin mit dem technischen Gemisch der Stearin- und Palmitinsäure, wie es aus Rindertalg gewonnen wird, mit sul- fierend wirkenden Mitteln behandelt.
Die neue Sulfonsäure bildet in Form ihrer Alkalisalze ein kaum gefärbtes Pulver mit ausgesprochen seifenartigen Eigenschaf ten. Sie soll als Hilfsstoff in der Textil industrie verwendet werden.
<I>Beispiel:</I> Man stellt ein Gemisch von Pentadecyl- und Heptadecylbenzimidazol durch Erwär men des technischen Gemisches von Stearin- Palmitinsäure, wie es aus Rindertalg ge wonnen wird, mit 41 Teilen .o-Phenylen- diamin her.
In 75 Teile Chlorsulfousäure, die auf 5 bis<B>10'</B> abgekühlt und gerührt werden, <I>trägt man</I> allmählich 25 Teile des Benzimid- azolgemisches ein und rührt das Gemisch bei 20 bis 25 so lange, bis eine herausgenom mene Probe sich in verdünnter Sodalösung klar auflöst.
Die Reaktionsmasse wird sodann in eis gekühlte gesättigte Kochsalzlösung ein gerührt, wobei das sulfonierte Produkt sich als eine nach kurzer Zeit erstarrende Masse abscheidet, die abgesaugt wird.
Das so erhaltene Produkt wird in heissem Wasser suspendiert, und durch Zusatz von Natronlauge neutralisiert, wobei eine klare, stark schäumende Lösung erhalten wird, aus der durch Eindampfen das Natriumsalz der entsprechenden Benzimidazol-sulfonsäure gewonnen wird.
Process for the preparation of a new sulfonic acid. It has been found that a new sulfonic acid is obtained if the imidazole mixture, which is formed by condensation of o-phenylenediamine with the technical mixture of stearic and palmitic acid, as it is obtained from beef tallow, is treated with sulphurizing agents .
In the form of its alkali salts, the new sulfonic acid forms a hardly colored powder with pronounced soap-like properties. It is intended to be used as an auxiliary in the textile industry.
<I> Example: </I> A mixture of pentadecylbenzimidazole and heptadecylbenzimidazole is produced by heating the technical mixture of stearic-palmitic acid, as it is obtained from beef tallow, with 41 parts of .o-phenylenediamine.
25 parts of the benzimidazole mixture are gradually introduced into 75 parts of chlorosulphous acid, which are cooled to 5 to 10 ′ and stirred, and the mixture is stirred at 20 to 25 for as long until a sample taken out dissolves clearly in dilute soda solution.
The reaction mass is then stirred into ice-cooled saturated sodium chloride solution, the sulfonated product separating out as a mass which solidifies after a short time and which is filtered off with suction.
The product obtained in this way is suspended in hot water and neutralized by adding sodium hydroxide solution, a clear, highly foaming solution being obtained from which the sodium salt of the corresponding benzimidazole sulfonic acid is obtained by evaporation.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH164736T | 1932-04-27 | ||
CH163005T | 1934-10-06 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH164736A true CH164736A (en) | 1933-10-15 |
Family
ID=25717675
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH164736D CH164736A (en) | 1932-04-27 | 1932-04-27 | Process for the preparation of a new sulfonic acid. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH164736A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE744281C (en) * | 1938-11-04 | 1944-01-18 | Phil Habil August Chwala Dipl | Process for the production of imidazoline-N-alkyl- or -oxyalkylsulfonic acids |
-
1932
- 1932-04-27 CH CH164736D patent/CH164736A/en unknown
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE744281C (en) * | 1938-11-04 | 1944-01-18 | Phil Habil August Chwala Dipl | Process for the production of imidazoline-N-alkyl- or -oxyalkylsulfonic acids |
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