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AT66528B - Process for the preparation of water-insoluble monoazo dyes. - Google Patents

Process for the preparation of water-insoluble monoazo dyes.

Info

Publication number
AT66528B
AT66528B AT66528DA AT66528B AT 66528 B AT66528 B AT 66528B AT 66528D A AT66528D A AT 66528DA AT 66528 B AT66528 B AT 66528B
Authority
AT
Austria
Prior art keywords
water
preparation
monoazo dyes
insoluble monoazo
parts
Prior art date
Application number
Other languages
German (de)
Original Assignee
Farbenfab Vorm Bayer F & Co
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 Farbenfab Vorm Bayer F & Co filed Critical Farbenfab Vorm Bayer F & Co
Application granted granted Critical
Publication of AT66528B publication Critical patent/AT66528B/en

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  • Paints Or Removers (AREA)

Description

  

   <Desc/Clms Page number 1> 
 
 EMI1.1 
 



   Es wurde gefunden, dass man zu wertvollen zur Herstellung von Lacken geeigneten Farbstoffen von sehr klaren, grünstichiggelben Tönen und guter Lichtechtheit dadurch gelangen 
 EMI1.2 
 bisher nur mit Hilfe von Mineralfarben herstellen konnte. 



   Beispiel l :
9'6 Teile   o-Chloranilin   werden mit 5 Teilen Natriumnitrit in bekannter Weise diazotiert. 



  Die klare Diazolösung lässt man darauf in eine Emulsion von 15 Teilen   Azetessig-p-anisidid nnd   1500 Teilen Wasser einfliessen, der soviel Natriumazetat zugefügt ist, dass die   Flüssigkeit   nicht 
 EMI1.3 
 mit Wasser gewaschen. 



   Der so erhaltene Farbstoff kann mit Wasser zu einer Paste   angerührt werden. (Getrocknet   bildet er ein Pulver von rein gelber Farbe. 



   Beispiel 2 :
11'8 Teile 2.5-Dichloranilin werden in bekannter Weise mit 5 Teilen Natriumnitrit diazotiert. 



    Die überschüssige   Säure der   Diazolösung   stumpft man am besten vorsichtig mit soviel Soda ah. dass die   Flüssigkeit   noch   kongosauer reagiert.   
 EMI1.4 
 ein Pulver von rein gelber Farbe. 



   Ersetzt man in vorstehenden Beispielen das o- ('hlor- bzw. das   2.     5-Di < 'hloranilin   z. B. durch p-Chlor-, o-Brom- oder 2,4-Dichloranilin usw., so entstehen Farbstoffe von   ähnlichen   Eigenschaften. 



   Die Kupplung verläuft in derselben Weise, wenn man ein für Lackfarben gebräuchliches Substrat, z. B. Schwerspat, zumischt. 



   Das Azetessig-p-anisidid vom Schmelzpunkt 115 bis 116  und das Azetessig-p-phenetidid vom Schmelzpunkt 103 bis 104  bilden weisse Kristalle, die sich leicht in Alkohol und warmem Benzol,   schwer in Äther lösen.   

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



   <Desc / Clms Page number 1>
 
 EMI1.1
 



   It has been found that valuable dyes suitable for the production of paints and having very clear, greenish-yellow tones and good lightfastness are thereby obtained
 EMI1.2
 was previously only able to produce with the help of mineral paints.



   Example l:
9'6 parts of o-chloroaniline are diazotized with 5 parts of sodium nitrite in a known manner.



  The clear diazo solution is then allowed to flow into an emulsion of 15 parts of acetoacetic acid-p-anisidide and 1500 parts of water, to which sufficient sodium acetate has been added that the liquid does not
 EMI1.3
 washed with water.



   The dye thus obtained can be mixed with water to form a paste. (When dried, it forms a powder that is pure yellow in color.



   Example 2:
11'8 parts of 2,5-dichloroaniline are diazotized in a known manner with 5 parts of sodium nitrite.



    The excess acid in the diazo solution is best blunted carefully with so much soda ah. that the liquid is still acidic in the Congo.
 EMI1.4
 a powder of pure yellow color.



   If, in the above examples, the o- ('chloro- or the 2. 5-di <' chloroaniline is replaced, for example, by p-chloro, o-bromo or 2,4-dichloroaniline, etc., dyes of similar properties.



   The coupling proceeds in the same way if one uses a substrate commonly used for paints, e.g. B. barite, admixed.



   Acetoacetic-p-anisidide with a melting point of 115 to 116 and acetoacetic-p-phenetidide with a melting point of 103 to 104 form white crystals that dissolve easily in alcohol and warm benzene, difficult in ether.

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

 

Claims (1)

PATENT-ANSPRUCH : Verfahren zur Darstellung von Lackfarbenstoffen, dadurch gekennzeichnet, dass man EMI1.5 **WARNUNG** Ende CLMS Feld Kannt Anfang DESC uberlappen**. PATENT CLAIM: Process for the representation of paint color substances, characterized in that one EMI1.5 ** WARNING ** End of CLMS field may overlap beginning of DESC **.
AT66528D 1912-06-07 1913-06-02 Process for the preparation of water-insoluble monoazo dyes. AT66528B (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE66528X 1912-06-07

Publications (1)

Publication Number Publication Date
AT66528B true AT66528B (en) 1914-09-10

Family

ID=5633471

Family Applications (1)

Application Number Title Priority Date Filing Date
AT66528D AT66528B (en) 1912-06-07 1913-06-02 Process for the preparation of water-insoluble monoazo dyes.

Country Status (1)

Country Link
AT (1) AT66528B (en)

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