CH150173A - Process for the preparation of a diazoamino compound. - Google Patents
Process for the preparation of a diazoamino compound.Info
- Publication number
- CH150173A CH150173A CH150173DA CH150173A CH 150173 A CH150173 A CH 150173A CH 150173D A CH150173D A CH 150173DA CH 150173 A CH150173 A CH 150173A
- Authority
- CH
- Switzerland
- Prior art keywords
- compound
- preparation
- diazoamino compound
- diazo
- diazoamino
- Prior art date
Links
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Darstellunz einer Diazoaminoverbindunz. Durch das Hauptpatent ist ein Verfahren zur Darstellung einer Diazoaminoverbindung beschrieben, dadurch gekennzeichnet, dass man die Diazoverbindung aus 3-Chloranilin auf 2-Amino-4-sulfobenzoesäure einwirken lässt.
Gegenstand vorliegender Erfindung ist nun ein Verfahren zur Darstellung einer Diazo- aminoverbindung, dadurch gekennzeichnet, dass man die Diazoverbindung aus 2. 5-Di- chloranilin auf 2-Naphtylamin-4.6.8-tri- sulfosäure einwirken lässt.
<I>Beispiel:</I> Die aus 161 Gewichtsteilen 2. 5-Dichlor- anilin in üblicher Weise mit Salzsäure und Natriumnitrit erhältliche Lösung von 2. 5- Dichlorbenzol-l-diazoniumchlorid lässt man in eine neutrale Lösung von 2-Naphtylamin- 4. 6.8-trisulfosäure einlaufen und stumpft die kongosaure Reaktion zweckmässig mit Natriumacetat ab.
Nach kurzer Zeit ist die Bildung der Diazoaminoverbindung von der Formel:
EMI0001.0025
vollendet, die sich auf Zusatz von Kochsalz als in Wasser leicht lösliches Natriumsalz abscheidet, das in üblicher Weise isoliert und getrocknet wird. Die Diazoaminoverbindung lässt sich in wässeriger Lösung durch Säuren leicht wieder in die Ausgangskomponenten spalten. Sie stellt ein in Wasser leicht lös liches gelbes Pulver dar, das in der Färberei- und Druckereipraxis, sowie als Schädlings bekämpfungsmittel Verwendung finden soll.
Process for the preparation of a diazoamino compound. The main patent describes a method for preparing a diazoamino compound, characterized in that the diazo compound from 3-chloroaniline is allowed to act on 2-amino-4-sulfobenzoic acid.
The present invention now relates to a process for preparing a diazoamino compound, characterized in that the diazo compound from 2,5-dichloroaniline is allowed to act on 2-naphthylamine-4,6,8-trisulfonic acid.
<I> Example: </I> The solution of 2.5-dichlorobenzene-1-diazonium chloride, which can be obtained from 161 parts by weight of 2.5-dichloro aniline in the usual way with hydrochloric acid and sodium nitrite, is left in a neutral solution of 2-naphthylamine 4. Run in 6.8-trisulfonic acid and expediently blunt the Congo acidic reaction with sodium acetate.
After a short time, the formation of the diazoamino compound has the formula:
EMI0001.0025
completed, which separates on the addition of common salt as a readily soluble sodium salt, which is isolated and dried in the usual way. The diazoamino compound can easily be split back into the starting components in aqueous solution by acids. It is a yellow powder that is easily soluble in water and is said to be used in dyeing and printing and as a pesticide.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE150173X | 1928-08-07 | ||
CH145151T | 1929-06-28 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH150173A true CH150173A (en) | 1931-10-15 |
Family
ID=25714611
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH150173D CH150173A (en) | 1928-08-07 | 1929-07-20 | Process for the preparation of a diazoamino compound. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH150173A (en) |
-
1929
- 1929-07-20 CH CH150173D patent/CH150173A/en unknown
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