CH227291A - Process for the production of a new sulfamide derivative. - Google Patents
Process for the production of a new sulfamide derivative.Info
- Publication number
- CH227291A CH227291A CH227291DA CH227291A CH 227291 A CH227291 A CH 227291A CH 227291D A CH227291D A CH 227291DA CH 227291 A CH227291 A CH 227291A
- Authority
- CH
- Switzerland
- Prior art keywords
- sulfamide derivative
- production
- new
- new sulfamide
- derivative
- Prior art date
Links
Classifications
-
- 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
- C07C311/01—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms
- C07C311/02—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C307/00—Amides of sulfuric acids, i.e. compounds having singly-bound oxygen atoms of sulfate groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C307/02—Monoamides of sulfuric acids or esters thereof, e.g. sulfamic acids
-
- 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
- C07C311/15—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Herstellung eines neuen Sulfamidderivates. Es wurde gefunden, dass man zu einem neuen Sulfamidderivat gelangt, wenn man N- Stearoyl-p-toluolsulfamid mit Natriumformal- dehydbisulfit in Abwesenheit eines Lösungs mittels umsetzt.
Die Umsetzung wird zweckmässig in der Wärme, z. B. bei 100-200 , vorgenommen, vorteilhaft in Gegenwart von reaktions beschleunigenden Stoffen, wie sekundären Aminen, beispielsweise unter Zusatz von Diamylamin.
Das neue Sulfamidderivat stellt eine feste Masse dar, die von heissem Wasser zu einer klaren, beim Schütteln stark schäumenden Lösung aufgenommen wird. Es kann als Textilhilfsstoff, z. B. als Waschmittel, An wendung finden.
<I>Beispiel:</I> 4,4 Gewichtsteile N-Stearoyl-p-toluolsulf- amid, 2 Gewichtsteile Natriumformaldehyd- bisulfit und 0,1 Gewichtsteil Diamylamin werden fein verrieben, während etwa 2 Stun den in einem Bad von 140-14511, während weiteren 2 Stunden in einem solchen von 155-160' und schliesslich in einem Bad von 180-190 gerührt. Das so erhaltene Reak tionsprodukt ist eine feste Masse, die von heissem Wasser zu einer klaren, beim Schüt teln stark schäumenden Lösung aufgenommen wird. Es kann als Textilhilfsstoff, z. B. als Waschmittel, Anwendung finden.
Process for the production of a new sulfamide derivative. It has been found that a new sulfamide derivative is obtained if N-stearoyl-p-toluenesulfamide is reacted with sodium formaldehyde bisulfite in the absence of a solvent.
The implementation is expediently in the heat, for. B. at 100-200, made, advantageously in the presence of reaction accelerating substances such as secondary amines, for example with the addition of diamylamine.
The new sulfamide derivative is a solid mass that is absorbed by hot water to form a clear, strongly foaming solution when shaken. It can be used as a textile auxiliary, e.g. B. as a detergent, to find application.
<I> Example: </I> 4.4 parts by weight of N-stearoyl-p-toluenesulphamide, 2 parts by weight of sodium formaldehyde bisulphite and 0.1 part by weight of diamylamine are finely ground for about 2 hours in a bath of 140-14511 , stirred for a further 2 hours in a bath of 155-160 'and finally in a bath of 180-190. The reaction product obtained in this way is a solid mass which is taken up by hot water to form a clear solution which foams strongly when shaken. It can be used as a textile auxiliary, e.g. B. as a detergent, use.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH227291T | 1941-07-02 | ||
CH225555T | 1941-07-02 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH227291A true CH227291A (en) | 1943-05-31 |
Family
ID=25726895
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH227291D CH227291A (en) | 1941-07-02 | 1941-07-02 | Process for the production of a new sulfamide derivative. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH227291A (en) |
-
1941
- 1941-07-02 CH CH227291D patent/CH227291A/en unknown
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