AT52976B - Process for the preparation of a dimethylbenzylphenylammonium monosulfonic acid. - Google Patents
Process for the preparation of a dimethylbenzylphenylammonium monosulfonic acid.Info
- Publication number
- AT52976B AT52976B AT52976DA AT52976B AT 52976 B AT52976 B AT 52976B AT 52976D A AT52976D A AT 52976DA AT 52976 B AT52976 B AT 52976B
- Authority
- AT
- Austria
- Prior art keywords
- dimethylbenzylphenylammonium
- monosulfonic acid
- acid
- preparation
- methylbenzylaniline
- Prior art date
Links
Landscapes
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Description
<Desc/Clms Page number 1>
Verfahren zur Darstellung einer Dimethylbenzylphenylammoniummonosulfosäure.
Es wurde gefunden, dass in dem Verfahren des Stammpatentes die Methylbenzylanilindisulfosäure durch die Methylbenzylanilinmonosulfosäure ersetzt werden kann, welche die Sulfogruppe im Benzylrest enthält. Die so erhaltene Dimethylbenzylphenylainnionium- monosulfosäure ist wie die Disulfosäure eine für Druckereizwecke sehr wertvolle Verbindung.
Sie ist in Wasser sehr leicht löslich. Beim Erwärmen dieser Lösung mit Athylanilin entsteht die bekannte Äthylbenzylanilinsulfosäure und Dimethylanilin.
Der Verbindung dürfte folgende Formel zukommen :
EMI1.1
Beispiel : 400 Teile einer Lösung von Methylbenzylanilinmonosulfosäure (Kalziumsalz), enthaltend 140 Teile Methylbenzylanilinsulfosäure, werden mit 95 Teilen p-Toluolsulfosäuremethylester und 10 Teilen Schlemmkreide unter gutem Umrühren solange auf 600 C erwärmt, bis der Sulfonsäureester verschwunden ist. Die so erhaltene Lösung kann entweder unmittelbar oder nach dem Abscheiden des Salzes der Toluolsulfosäure zur Trockne verdampft werden.
**WARNUNG** Ende DESC Feld kannt Anfang CLMS uberlappen**.
<Desc / Clms Page number 1>
Process for the preparation of a dimethylbenzylphenylammonium monosulfonic acid.
It has been found that in the process of the parent patent the methylbenzylaniline disulfonic acid can be replaced by the methylbenzylaniline monosulfonic acid, which contains the sulfo group in the benzyl radical. The dimethylbenzylphenylainnionium monosulfonic acid obtained in this way, like the disulfonic acid, is a very valuable compound for printing purposes.
It is very easily soluble in water. When this solution is heated with ethylaniline, the well-known ethylbenzylaniline sulfonic acid and dimethylaniline are produced.
The compound should have the following formula:
EMI1.1
Example: 400 parts of a solution of methylbenzylaniline monosulfonic acid (calcium salt) containing 140 parts of methylbenzylaniline sulfonic acid, 95 parts of methyl p-toluenesulfate and 10 parts of chalk are heated to 600 C with thorough stirring until the sulfonic acid ester has disappeared. The solution obtained in this way can be evaporated to dryness either immediately or after the salt of toluenesulfonic acid has separated out.
** WARNING ** End of DESC field may overlap beginning of CLMS **.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AT52974X | 1910-03-22 | ||
DE52976X | 1910-11-21 |
Publications (1)
Publication Number | Publication Date |
---|---|
AT52976B true AT52976B (en) | 1912-04-10 |
Family
ID=25602035
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AT52976D AT52976B (en) | 1910-03-22 | 1911-03-18 | Process for the preparation of a dimethylbenzylphenylammonium monosulfonic acid. |
Country Status (1)
Country | Link |
---|---|
AT (1) | AT52976B (en) |
-
1911
- 1911-03-18 AT AT52976D patent/AT52976B/en active
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