CH180577A - Process for the production of a new textile auxiliary. - Google Patents
Process for the production of a new textile auxiliary.Info
- Publication number
- CH180577A CH180577A CH180577DA CH180577A CH 180577 A CH180577 A CH 180577A CH 180577D A CH180577D A CH 180577DA CH 180577 A CH180577 A CH 180577A
- Authority
- CH
- Switzerland
- Prior art keywords
- group
- converted
- production
- sulfuric acid
- textile auxiliary
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C305/00—Esters of sulfuric acids
- C07C305/02—Esters of sulfuric acids having oxygen atoms of sulfate groups bound to acyclic carbon atoms of a carbon skeleton
- C07C305/04—Esters of sulfuric acids having oxygen atoms of sulfate groups bound to acyclic carbon atoms of a carbon skeleton being acyclic and saturated
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/30—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/37—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups having the sulfur atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Detergent Compositions (AREA)
Description
Verfahren zur Herstellung eines neuen Textilhilfsstoffes. Es wurde gefunden, dass man ein ka- pillaraktives Kondensationsprodukt erhält, wenn man ausgehend vom 1-Chlor-4-nitro- henzol-2-sulfonsäure-N-oxyä-thylamid einer seits die Nitrogruppe durch ein Reduktions mittel in eine Aminogruppe und letztere hierauf durch ein Oleylierungsmittel in eine Oleylaminogruppe,
anderseits die Oxyäthyl- amidgruppe mittels Schwefelsäure in den Schwefelsäureester dieser Gruppe überführt. Das so erhaltene Produkt bildet in trockenem Zustande ein helles Pulver, das sich in war mem Wasser unter Bildung einer stark schäumenden Lösung, die eine ausgezeich nete Netz- und Waschwirkung besitzt, auf löst.
<I>Beispiel:</I> Durch Eintragen von 256 Teilen 1-Chlor- 4-nitrobenzol-2-sulfonsäurechlorid in eine wässerige Lösung von 122 Teilen Äthanol amin stellt man in üblicher Weise das 1- Chlor-4-nitrobenzol-2-sulfonsäureoxäthvlamid her. 281 Teile dieses Körpers werden bei 10 bis 20 in 1100 Teile 100 % ige Schwefel säure eingetragen.
Die erhaltene Lösung giesst man in zirka '3000 Teile konzentrierte Chlornatriumlösung, wobei nach einigem Rühren in der Kälte das Natriumsalz des Sehwefelsäureesters des 1-Chlor-4-nitroben- zol - 2. - sulfonsäureoxyäthylamids ausfällt.
Durch Reduktion mit Eisen in wässeriger Lösung nach üblichen Methoden erhält man die entsprechende 4-Aminoverbindung. In eine Lösung von 440 Teilen des so gewon nenen Aminokörpers und 82, Teilen Natrium acetat in 800 Teilen Wasser lässt man bei 5 bis 15 300 Teile Olsäurechlorid eintropfen. Hierauf wird mit Natriumhydroxyd neutral gestellt und 2 bis 3 Stunden bei Zimmertem peratur nachgerührt. Das erhaltene Produkt kann in bekannter Weise auf Pasten oder Trockenpulver verarbeitet werden.
Process for the production of a new textile auxiliary. It has been found that a capillary-active condensation product is obtained if, starting from 1-chloro-4-nitrohenenzene-2-sulfonic acid-N-oxyethylamide, on the one hand, the nitro group is converted into an amino group by means of a reducing agent and the latter is then converted by an oleylating agent into an oleylamino group,
on the other hand, the oxyethyl amide group is converted into the sulfuric acid ester of this group by means of sulfuric acid. The product thus obtained forms a pale powder when dry, which dissolves in warm water to form a strongly foaming solution which has excellent wetting and washing properties.
<I> Example: </I> By introducing 256 parts of 1-chloro-4-nitrobenzene-2-sulfonic acid chloride into an aqueous solution of 122 parts of ethanolamine, the 1- chloro-4-nitrobenzene-2- sulfonic acid oxyethylene amide. 281 parts of this body are entered at 10 to 20 in 1100 parts of 100% sulfuric acid.
The resulting solution is poured into about 3000 parts of concentrated sodium chloride solution, and after some stirring in the cold, the sodium salt of the sulfuric acid ester of 1-chloro-4-nitrobenzene-2-sulfonic acidoxyethyl amide precipitates.
The corresponding 4-amino compound is obtained by reduction with iron in aqueous solution by customary methods. In a solution of 440 parts of the amino body won in this way and 82 parts of sodium acetate in 800 parts of water, 5 to 15,300 parts of oleic acid chloride are added dropwise. It is then made neutral with sodium hydroxide and stirred for 2 to 3 hours at room temperature. The product obtained can be processed into pastes or dry powder in a known manner.
Claims (1)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH178533T | 1934-02-13 | ||
| CH180577T | 1934-02-13 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH180577A true CH180577A (en) | 1935-10-31 |
Family
ID=25720124
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH180577D CH180577A (en) | 1934-02-13 | 1934-02-13 | Process for the production of a new textile auxiliary. |
Country Status (1)
| Country | Link |
|---|---|
| CH (1) | CH180577A (en) |
-
1934
- 1934-02-13 CH CH180577D patent/CH180577A/en unknown
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