AT72940B - Process for the preparation of yellow chromating dyes. - Google Patents

Process for the preparation of yellow chromating dyes.

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Publication number
AT72940B
AT72940B AT72940DA AT72940B AT 72940 B AT72940 B AT 72940B AT 72940D A AT72940D A AT 72940DA AT 72940 B AT72940 B AT 72940B
Authority
AT
Austria
Prior art keywords
dyes
preparation
yellow chromating
chromating
yellow
Prior art date
Application number
Other languages
German (de)
Original Assignee
Hoechst Ag
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Hoechst Ag filed Critical Hoechst Ag
Application granted granted Critical
Publication of AT72940B publication Critical patent/AT72940B/en

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Description

  

   <Desc/Clms Page number 1> 
 



  Verfahren zur Darstellung gelber Chromierfarbstoffe. 



   Es wurde gefunden, dass man zu gelben Chromierfarbstoffen gelangt, wenn man Anthrauilsäure oder deren   Substitutionsprodukte   mit   Pyrazolonsulfosäuren   oder deren Derivaten kuppelt. 



  Die Farbstoffe zeichnen sich durch hervorragende Karbonisierechtheit und durch sehr gute Walkechtheit aus. 



   Beispiele :
1.    171'5   Teile 5-Chlor-2-aminobenzoesäure werden in der üblichen Weise diazotiert. 



  Man   lässt   die   Uiazolösung   in eine   sodaalkalische Auflösung von 288#5 Teilen 1 (2-Chlor-   -5-sulfophenyl)-3-methyl-5-pyrazolon fliessen und fällt nach beendigter Kupplung den Farbstoff mit Salz. 
 EMI1.1 
 säure mit einer sodaalkalischen Lösung von 254 Teile 1 (p-Sulfophenyl)-3-methyl-5-pyrazolon. 



  Der Farbstoff wird ausgesalzen und wie   üblich aufgearbeitet.   

**WARNUNG** Ende DESC Feld kannt Anfang CLMS uberlappen**.



   <Desc / Clms Page number 1>
 



  Process for the preparation of yellow chromating dyes.



   It has been found that yellow chromating dyes are obtained when anthrauilic acid or its substitution products are coupled with pyrazolone sulfonic acids or their derivatives.



  The dyes are characterized by excellent carbonization fastness and very good milled fastness.



   Examples:
1. 171'5 parts of 5-chloro-2-aminobenzoic acid are diazotized in the usual way.



  The uiazo solution is allowed to flow into a soda-alkaline solution of 288 # 5 parts of 1 (2-chloro--5-sulfophenyl) -3-methyl-5-pyrazolone and, after coupling is complete, the dye is precipitated with salt.
 EMI1.1
 acid with a soda-alkaline solution of 254 parts of 1 (p-sulfophenyl) -3-methyl-5-pyrazolone.



  The dye is salted out and worked up as usual.

** WARNING ** End of DESC field may overlap beginning of CLMS **.

 

Claims (1)

EMI1.2 Verfahren zur Darstellung gelber Chromierfarbstoffe, dadurch gekennzeichnet, dass man die Diazovorbindung aus Anthranilsäuro oder deren Substitutionsprodukten auf Pyrazolon- sulfosäuren oder deren Derivatve einwirken lässt. **WARNUNG** Ende CLMS Feld Kannt Anfang DESC uberlappen**. EMI1.2 Process for the preparation of yellow chromating dyes, characterized in that the diazo pre-bond from anthranilic acid or its substitution products is allowed to act on pyrazolone sulfonic acids or their derivatives. ** WARNING ** End of CLMS field may overlap beginning of DESC **.
AT72940D 1913-11-05 1914-07-13 Process for the preparation of yellow chromating dyes. AT72940B (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE72940X 1913-11-05

Publications (1)

Publication Number Publication Date
AT72940B true AT72940B (en) 1917-01-10

Family

ID=5636305

Family Applications (1)

Application Number Title Priority Date Filing Date
AT72940D AT72940B (en) 1913-11-05 1914-07-13 Process for the preparation of yellow chromating dyes.

Country Status (1)

Country Link
AT (1) AT72940B (en)

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