CH178533A - Process for the production of a new textile auxiliary. - Google Patents
Process for the production of a new textile auxiliary.Info
- 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
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)
- 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)
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) |
-
1934
- 1934-02-13 CH CH178533D patent/CH178533A/en unknown
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CH178533A (en) | Process for the production of a new textile auxiliary. | |
CH180576A (en) | Process for the production of a new textile auxiliary. | |
CH180578A (en) | Process for the production of a new textile auxiliary. | |
CH180577A (en) | Process for the production of a new textile auxiliary. | |
CH256767A (en) | Process for the production of a new half-ester. | |
AT160231B (en) | Process for the manufacture of products containing sulfuric acid residues. | |
CH156307A (en) | Process for the preparation of a sulfuric acid ester. | |
CH193924A (en) | Process for the production of a new textile auxiliary. | |
CH179442A (en) | Process for the production of a new textile auxiliary. | |
CH187421A (en) | Process for the production of a new textile auxiliary. | |
CH229186A (en) | Process for the preparation of the di (sulfuric acid ester) of 1,4-di (oxäthylamino) -6-chloroanthraquinone. | |
CH182586A (en) | Process for the preparation of a heterocyclic amino compound. | |
CH182592A (en) | Process for the preparation of an amine oxide. | |
CH189302A (en) | Process for the production of a new textile auxiliary. | |
CH168725A (en) | Process for the preparation of a new ester acid. | |
CH181156A (en) | Process for the production of a new textile auxiliary. | |
CH153675A (en) | Process for the preparation of a condensation product which can be used as a reservation agent. | |
CH177819A (en) | Process for the preparation of 4-trifluoromethyl-2-aminophenylmethylsulfone. | |
CH189136A (en) | Process for the production of a new textile auxiliary. | |
CH177458A (en) | Process for the preparation of an amine oxide. | |
CH191412A (en) | Process for the production of a new textile auxiliary. | |
CH240356A (en) | Process for the production of a water-soluble, higher molecular weight guanamine. | |
CH159030A (en) | Process for the production of an ammonium salt. | |
CH189030A (en) | Process for the preparation of 2-methyl-amino-4-chlorophenol. | |
CH189031A (en) | Process for the preparation of 2-methyl-amino-1-naphthol. |