CH178533A - Process for the production of a new textile auxiliary. - Google Patents

Process for the production of a new textile auxiliary.

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Publication number
CH178533A
CH178533A CH178533DA CH178533A CH 178533 A CH178533 A CH 178533A CH 178533D A CH178533D A CH 178533DA CH 178533 A CH178533 A CH 178533A
Authority
CH
Switzerland
Prior art keywords
group
converted
production
sulfuric acid
textile auxiliary
Prior art date
Application number
Other languages
German (de)
Inventor
Gesellschaft Fuer Chemis Basel
Original Assignee
Chem Ind Basel
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Chem Ind Basel filed Critical Chem Ind Basel
Publication of CH178533A publication Critical patent/CH178533A/en

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C305/00Esters of sulfuric acids
    • C07C305/02Esters of sulfuric acids having oxygen atoms of sulfate groups bound to acyclic carbon atoms of a carbon skeleton
    • C07C305/04Esters of sulfuric acids having oxygen atoms of sulfate groups bound to acyclic carbon atoms of a carbon skeleton being acyclic and saturated
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C311/00Amides 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
    • C07C311/30Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups
    • C07C311/37Sulfonamides, 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

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Description

  

  Verfahren zur Herstellung eines neuen     Tegtilhilfsstoffes.       Es wurde gefunden, dass man ein kapillar  aktives Kondensationsprodukt erhält, wenn  man ausgehend vom     1-Nitrobenzol-3-sulfon-          säure-N-oxyäthylamid    einerseits die     Nitro-          gruppe    durch ein Reduktionsmittel in eine       Aminogrupppe    und letztere hierauf durch ein       Lauroylierungsmittel    in eine     Lauroylamino-          gruppe,

      anderseits die     Oxyäthylamidgruppe          mittelst    Schwefelsäure in den     Schwefelsäure-          ester    dieser Gruppe überführt. Das so er  haltene Produkt bildet in trockenem     Zustande     ein     reinweisses    Pulver, das sich in warmem  Wasser unter Bildung einer stark schäumen  den Lösung, die eine ausgezeichnete     Netz-          und    Waschwirkung besitzt, auflöst.  



  <I>Beispiel</I>  Durch Eintragen von 221 Teilen     1-Nitr-o-          benzol-3-sulfonsäurechlorid    in eine wässerige  Lösung von 122 Teilen     Äthanolamin    stellt  man in üblicher Weise das     1-Nitro        3-benzol-          sirlfonsäureoxäthylamid    her. 246 Teile dieses  Körpers werden bei 10-200 in 1000 Teile         1000%ige    Schwefelsäure eingetragen.

   Die er  haltene Lösung giesst man in ca. 3000 Teile  konzentrierte     Ohlornatriumlösung,    wobei nach  einigem Rühren in der Kälte das Natrium  salz des     Schwefelsäureesters    des     1-Nitro-3-          benzolsulfonsäureoxäthylamids    ausfällt.

   Durch  Reduktion mit Eisen in wässeriger Lösung  nach üblichen Methoden erhält man die ent  sprechende     1-Aminoverbindung.    In eine Lö  sung von 380 Teilen des so gewonnenen       Aminokörpers    und 82 Teilen     Natriumacetat     in<B>800</B> Teilen Wasser lässt man bei 5-15 0  218 Teile     Laurylsäurechlorid        eintropfen.    Hier  auf wird     cnit        Natriumhydroxyd    neutral ge  stellt und 2 bis 3 Stunden bei Zimmertempe  ratur nachgerührt. Das erhaltene Produkt  kann in bekannter Weise auf Pasten oder  Trockenpulver verarbeitet werden. .



  Process for the production of a new Tegtil auxiliary. It has been found that a capillary active condensation product is obtained if, starting from 1-nitrobenzene-3-sulfonic acid-N-oxyethylamide, on the one hand the nitro group is converted into an amino group by a reducing agent and the latter is then converted into a lauroylamino group by a lauroylating agent group,

      on the other hand, the oxyethylamide group is converted into the sulfuric acid ester of this group by means of sulfuric acid. The product obtained in this way forms a pure white 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 221 parts of 1-nitr-o-benzene-3-sulfonic acid chloride into an aqueous solution of 122 parts of ethanolamine, 1-nitro-3-benzene-sulfonic acid oxethylamide is prepared in the usual way. 246 parts of this body are entered at 10-200 in 1000 parts of 1000% sulfuric acid.

   The solution he obtained is poured into about 3000 parts of concentrated sodium carbonate solution, and after some stirring in the cold, the sodium salt of the sulfuric acid ester of 1-nitro-3-benzenesulfonic acid oxäthylamide precipitates.

   The corresponding 1-amino compound is obtained by reduction with iron in aqueous solution by customary methods. In a solution of 380 parts of the amino body obtained in this way and 82 parts of sodium acetate in 800 parts of water, 5-15 0 218 parts of lauric acid chloride are added dropwise. Here it is 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)

PATENTANSPRUCH: Verfahren zur Herstellung eines neuen Textilhilfsstoffes, dadurch gekennzeichnet, dass man ausgehend vom 1-Nitrobenzol-3-sulfon- säure-N-oxyäthylamid einerseits die Nitro- gruppe durch ein Reduktionsmittel in eine Aminogruppe und letztere hierauf durch ein Lauroylierungsmittel in eine Lauroylamino- gruppe, anderseits die Oxyäthylaminogruppe mittelst Schwefelsäure in den Schwefelsäure ester dieser Gruppe überführt. PATENT CLAIM: Process for the production of a new textile auxiliary, characterized in that starting from 1-nitrobenzene-3-sulfonic acid-N-oxyethylamide, on the one hand, the nitro group is converted into an amino group by a reducing agent and the latter is then converted into a lauroylamino group by a lauroylating agent. group, on the other hand the oxyethylamino group is converted into the sulfuric acid ester of this group by means of sulfuric acid. Das so er- haltere Produkt bildet in trockenem Zustande ein reinweisses Pulver, das sich in warmem Wasser unter Bildung einer stark schäumen den Lösung, die eine ausgezeichnete Netz-, Wasch- und Egalisierwirkung besitzt, auflöst. The product obtained in this way forms a pure white powder when dry, which dissolves in warm water to form a strongly foaming solution which has excellent wetting, washing and leveling properties.
CH178533D 1934-02-13 1934-02-13 Process for the production of a new textile auxiliary. CH178533A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH178533T 1934-02-13

Publications (1)

Publication Number Publication Date
CH178533A true CH178533A (en) 1935-07-31

Family

ID=4428579

Family Applications (1)

Application Number Title Priority Date Filing Date
CH178533D CH178533A (en) 1934-02-13 1934-02-13 Process for the production of a new textile auxiliary.

Country Status (1)

Country Link
CH (1) CH178533A (en)

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