CH235195A - Process for the preparation of a new derivative of an aminodisulfonic acid. - Google Patents
Process for the preparation of a new derivative of an aminodisulfonic acid.Info
- Publication number
- CH235195A CH235195A CH235195DA CH235195A CH 235195 A CH235195 A CH 235195A CH 235195D A CH235195D A CH 235195DA CH 235195 A CH235195 A CH 235195A
- Authority
- CH
- Switzerland
- Prior art keywords
- acid
- aminodisulfonic
- preparation
- new derivative
- new
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
- C07C309/01—Sulfonic acids
- C07C309/28—Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
- C07C309/45—Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing nitrogen atoms, not being part of nitro or nitroso groups, bound to the carbon skeleton
- C07C309/47—Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing nitrogen atoms, not being part of nitro or nitroso groups, bound to the carbon skeleton having at least one of the sulfo groups bound to a carbon atom of a six-membered aromatic ring being part of a condensed ring system
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Detergent Compositions (AREA)
Description
Verfahren zur Herstellung eines neuen Derivates einer Aminoclisulfonsäure. Es vulrde befunden, dass man zu einem neuen Derivat einer Aminodisulfonsäure be langt, wenn man 1. 11o1 2,6,8-Naphthylamin- disulfonsäure mit 1 Mol ar-2-Chlormethyl- tetrahyd@ronaphthalin in Gegenwart eines säurebindenden Mittels umsetzt.
Die Umsetzung wird zweckmässig bei 60 bis 75 vorgenommen. wobei man als säure- liiudendesMittel vorteilhaft Natriumcarbonai verwendet.
Das Dinatriumsalz des neuen Erzeub- nis#ses bildet ein gelblich gefärbtes Pulver, das in Wasser mit schwach grüner Fluores zenz klar löslich ist und gute Schaum- und Wascheigenschaften besitzt. Es kann als Textilhilfsstoff, z. B.* als Waschmittel, An wendung finden.
<I>Beispiel:</I> In eine Lösung von 347 Gewichtsteilen des Dinatriumsalzes der 2,6,8-Naphthyl- amindisulfoii,c_äure in 500 Volumteilen Was ser werden bei 70-75 unter Rühren 180 Ge- wichtsteile ar- -Ch.lormethyl-tetrahydronaph- thalin (1 11.1o1,
innerhalb zwei Stunden ein- betragen und bleichzeitig so viel Natrium- carbonat zusefiigt, dass die Reaktionsmasse stets schwach alkalisch reagiert. Nachdem alles ar-2-Chlormethy 1-tetrahydronaplithalin einbetragen ist und kein Alkali mehr ver braucht wird, rührt man noch einige Stun den bei der gleichen Temperatur weiter, stellt hierauf neutral und da.mpfl-..die entstandene klare Lösun'. zur Trockne ein.
Das auf diese Weise erhaltene Aralkvlie- rungsprodukt bildet- ein gelblich gefärbtes Pulver, das in Wasser mit schwach grüner Fluoreszenz klar löslich ist und gute Schaum und Wascheigenschaften besitzt.
Process for the preparation of a new derivative of an aminoclisulfonic acid. It has generally been found that a new derivative of an aminodisulfonic acid is obtained if 1,111 2,6,8-naphthylamino-disulfonic acid is reacted with 1 mol of ar-2-chloromethyl-tetrahydronaphthalene in the presence of an acid-binding agent.
The reaction is conveniently carried out at 60 to 75. Sodium carbonate is advantageously used as the acid-releasing agent.
The disodium salt of the new product forms a yellowish colored powder that is clearly soluble in water with a slightly green fluorescence and has good foam and washing properties. It can be used as a textile auxiliary, e.g. B. * as a detergent, to find application.
<I> Example: </I> In a solution of 347 parts by weight of the disodium salt of 2,6,8-naphthylamine disulfoii, c_acid in 500 parts by volume of water, 180 parts by weight of ar- -Ch. lormethyl-tetrahydronaphthalene (1 11.101,
be in within two hours and at the same time add enough sodium carbonate that the reaction mass always reacts weakly alkaline. After all the ar-2-chloromethyl 1-tetrahydronaplithalin has been entered and no more alkali has been used, the mixture is stirred for a few more hours at the same temperature, then neutralized and the resulting clear solution. to dry up.
The aralkvlaze product obtained in this way forms a yellowish colored powder which is clearly soluble in water with a weak green fluorescence and which has good foam and washing properties.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH232114T | 1941-12-24 | ||
CH235195T | 1941-12-24 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH235195A true CH235195A (en) | 1944-11-15 |
Family
ID=25727664
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH235195D CH235195A (en) | 1941-12-24 | 1941-12-24 | Process for the preparation of a new derivative of an aminodisulfonic acid. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH235195A (en) |
-
1941
- 1941-12-24 CH CH235195D patent/CH235195A/en unknown
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