CH196533A - Process for the production of a new textile auxiliary product. - Google Patents
Process for the production of a new textile auxiliary product.Info
- Publication number
- CH196533A CH196533A CH196533DA CH196533A CH 196533 A CH196533 A CH 196533A CH 196533D A CH196533D A CH 196533DA CH 196533 A CH196533 A CH 196533A
- Authority
- CH
- Switzerland
- Prior art keywords
- production
- auxiliary product
- textile auxiliary
- way
- new textile
- 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
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D233/84—Sulfur atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Description
Verfahren zur Herstellung eines neuen Tegtilhilfsproduktes. Es wurde gefunden, dass man eine neue Sulfonsäure erhält, wenn man das ,u-n-Hep- tadecylbenzimidazol, das beispielsweise ent steht durch Kondensieren von o-Phenylen- diamin mit Stearinsäure, zunächst einer Me- thylierung durch Behandeln im geschlossenen Gefäss mit überschüssigem Chlormethyl bei Temperaturen, die zwischen 140 und<B>180'</B> liegen,
unterwirft und hierauf das so erhal tene Produkt mit sulfierend wirkenden Mitteln behandelt.
Die so erhaltene Sulfonsäure bildet in Form ihrer Alkalisalze ein kaum gefärbtes Pulver, dessen wässerige Lösungen hervor ragende kapillaraktive Eigenschaften auf weisen.
<I>Beispiel:</I> Zu 71 Teilen ss-n-Heptadecylbenzimidazol werden in einem Autoklaven 30 Teile Chlor methyl gepresst, worauf das Reaktionsgemisch während 14 Stunden auf 155-1600 erhitzt wird. Nach dem Erkalten bildet das Reak tionsprodukt eine feste fettige Masse, die in Wasser spielend löslich ist. 200 Teile des so erhaltenen Methylierungs- produktes werden zu 400 Teilen Schwefel säure bei<B>10-15'</B> allmählich zugefügt.
Nach dem eine homogene Mischung entstanden ist, kühlt man das Gemisch auf --f- 5 0 ab und führt nun die Sulfonierung bei -(- 5 0 bis 10 durch, indem man langsam 380-385 Teile Oleum (24% SO, 9-Gehalt) zufliessen lässt. Die Sulfonierung ist beendet, wenn eine Probe der Masse in verdünnter Natriumcar- bonatlösung völlig klar löslich ist.
Nun giesst man die Sulfonierungsmasse unter Rühren auf 2400 Teile Eis, wobei die Sulfonsäure ausfällt und von der wässerigen Schwefel säure abfiltriert und gewaschen werden kann. Nach dem Neutralisieren der so erhaltenen Sulfonsäure mit Natriumhydroaydlösung und Eindampfen der Lösung im Vakuum erhält man das Natriumsalz der Sulfosäure als ein in Wasser sehr leicht lösliches Pulver.
Process for the production of a new Tegtil auxiliary product. It has been found that a new sulfonic acid is obtained if the un-heptadecylbenzimidazole, which is formed, for example, by condensing o-phenylenediamine with stearic acid, is first methylated by treating it in a closed vessel with excess chloromethyl Temperatures between 140 and <B> 180 '</B>,
and then treated the product obtained in this way with sulphurizing agents.
The sulfonic acid obtained in this way, in the form of its alkali metal salts, forms a hardly colored powder, the aqueous solutions of which have excellent capillary-active properties.
<I> Example: </I> To 71 parts of ss-n-heptadecylbenzimidazole, 30 parts of chloromethyl are pressed in an autoclave, whereupon the reaction mixture is heated to 155-1600 for 14 hours. After cooling, the reaction product forms a solid, fatty mass that is easily soluble in water. 200 parts of the methylation product thus obtained are gradually added to 400 parts of sulfuric acid at <B> 10-15 '</B>.
After a homogeneous mixture has formed, the mixture is cooled to --f- 5 0 and the sulfonation is now carried out at - (- 5 0 to 10 by slowly adding 380-385 parts of oleum (24% SO, 9- The sulfonation is complete when a sample of the mass is completely soluble in dilute sodium carbonate solution.
The sulfonation mass is then poured onto 2400 parts of ice with stirring, the sulfonic acid precipitating and the aqueous sulfuric acid can be filtered off and washed. After neutralizing the sulfonic acid obtained in this way with sodium hydroxide solution and evaporating the solution in vacuo, the sodium salt of the sulfonic acid is obtained as a powder which is very easily soluble in water.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH196533T | 1937-01-14 | ||
CH163274T | 1937-01-14 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH196533A true CH196533A (en) | 1938-03-15 |
Family
ID=25717728
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH196533D CH196533A (en) | 1937-01-14 | 1937-01-14 | Process for the production of a new textile auxiliary product. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH196533A (en) |
-
1937
- 1937-01-14 CH CH196533D patent/CH196533A/en unknown
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