AT57429B - Process for the preparation of new vat dyes. - Google Patents

Process for the preparation of new vat dyes.

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Publication number
AT57429B
AT57429B AT57429DA AT57429B AT 57429 B AT57429 B AT 57429B AT 57429D A AT57429D A AT 57429DA AT 57429 B AT57429 B AT 57429B
Authority
AT
Austria
Prior art keywords
preparation
vat dyes
new vat
dyes
parts
Prior art date
Application number
Other languages
German (de)
Original Assignee
Chem Ind Basel
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 Chem Ind Basel filed Critical Chem Ind Basel
Application granted granted Critical
Publication of AT57429B publication Critical patent/AT57429B/en

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  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Description

  

   <Desc/Clms Page number 1> 
 



  Verfahren zur Darstellung neuer   KOpenfarb8toft'e.   



   Ei wurde gefunden, dass man zu wertvollen Küpenfarbstoffen gelangt, wenn man die Kondensationsprodukte aus Azenaphtenchinon oder dessen Substitutionsprodukten mit 6-Amido- -3-oxy-(1)-thionaphten-2-karbonsäuren bzw. 6-Amino-3-oxy-(1)-thionaphtenen der Halogenierung unterwirft. Die so erhältlichen Farbstoffe färben aus alkalischer Küpe sowohl Baumwolle als auch Wolle orange bis bräunlich-orange. 



   Beispiel 1. 



   Itr ein auf 0  C abgekühltes Gemisch von 80 Teilen Schwefelsliure 1 970/0 und 7 Teilen Brom werden unter gutem Rühren    3" Teile dAS   durch Kondensation von Azenaphtenchinon mit 6-Amino-3-oxy-   (1) -thionaphten   in Alkohol erhältuchen Produkts 
 EMI1.1 
 besitzen eine lebhafte orange Nuance. 



   Beispiel 2. 



     3#7   Teile des durch Kondensation von 6-Amino-3-oxy-1-thionaphtenkarbonsäure mit 
 EMI1.2 
 3r) bis 40 Teilen Nitrobenzol suspendiert, 7 Teile Brom hinzugefügt, worauf die Mischung während zwölf Stunden bei gewöhnlicher Temperatur durchgerührt wird. Sodann erwärmt man noch ein bis zwei Stunden auf 200 bis 220  C, lässt erkalten und filtriert das ausgeschiedene Bromieruugsprodukt ab. Der neue Farbstoff   wir (i   in Form eines   braungelbon   Pulvers erhalten, das sich in konzentrierter Schwefelsäure mit grünlich-blauer Farbe löst. 



  Seine Küpenfärbungen besitzen   bräunlich-orange   Nuance. 



   In analoger Weise erfolgt die Darstellung von Farbstoffen unter Verwendung von 
 EMI1.3 
 A minoazenaphtenchinon. 

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



   <Desc / Clms Page number 1>
 



  Procedure for displaying new KOpenfarb8toft'e.



   It has been found that valuable vat dyes can be obtained if the condensation products of azenaphthenequinone or its substitution products with 6-amido- -3-oxy- (1) -thionaphten-2-carboxylic acids or 6-amino-3-oxy- ( 1) -thionaphtenes subject to halogenation. The dyes obtainable in this way dye both cotton and wool from an alkaline vat from orange to brownish-orange.



   Example 1.



   A mixture, cooled to 0 ° C., of 80 parts of sulfuric acid 1970/0 and 7 parts of bromine is obtained, with thorough stirring, by condensing azenaphtenquinone with 6-amino-3-oxy- (1) -thionaphthene in alcohol
 EMI1.1
 have a lively orange shade.



   Example 2.



     3 # 7 parts of the by condensation of 6-amino-3-oxy-1-thionaphtenecarboxylic acid with
 EMI1.2
 3r) suspended up to 40 parts of nitrobenzene, added 7 parts of bromine, whereupon the mixture is stirred for twelve hours at ordinary temperature. The mixture is then heated to 200 to 220 ° C. for one to two hours, allowed to cool and the precipitated bromination product is filtered off. The new dye is obtained in the form of a brownish-yellow powder that dissolves in concentrated sulfuric acid with a greenish-blue color.



  Its vat colors have a brownish-orange shade.



   The representation of dyes takes place in an analogous manner using
 EMI1.3
 A minoazenaphthene quinone.

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

 

Claims (1)

An Stelle der in Beispiel 1 und 2 genannten Verdünnungsmittel kann man auch EMI1.4 mittel benutzt werden. rATENT AXSt' ('H : Verfahren zur Herstellung von @üpenfarbstoffen, dadurch gekennzeichnet. dass man EMI1.5 **WARNUNG** Ende CLMS Feld Kannt Anfang DESC uberlappen**. Instead of the diluents mentioned in Examples 1 and 2, it is also possible to use EMI1.4 medium can be used. RATENT AXSt '(' H: Process for the production of @uene dyes, characterized. that he EMI1.5 ** WARNING ** End of CLMS field may overlap beginning of DESC **.
AT57429D 1910-10-28 1911-10-12 Process for the preparation of new vat dyes. AT57429B (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR57429X 1910-10-28

Publications (1)

Publication Number Publication Date
AT57429B true AT57429B (en) 1913-01-25

Family

ID=8691478

Family Applications (1)

Application Number Title Priority Date Filing Date
AT57429D AT57429B (en) 1910-10-28 1911-10-12 Process for the preparation of new vat dyes.

Country Status (1)

Country Link
AT (1) AT57429B (en)

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