AT41780B - Process for the production of orange vat dyes. - Google Patents

Process for the production of orange vat dyes.

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Publication number
AT41780B
AT41780B AT41780DA AT41780B AT 41780 B AT41780 B AT 41780B AT 41780D A AT41780D A AT 41780DA AT 41780 B AT41780 B AT 41780B
Authority
AT
Austria
Prior art keywords
production
orange
vat dyes
bromine
dye
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
Priority claimed from DE1907198644D external-priority patent/DE198644C/de
Application filed by Hoechst Ag filed Critical Hoechst Ag
Application granted granted Critical
Publication of AT41780B publication Critical patent/AT41780B/en

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Description

  

   <Desc/Clms Page number 1> 
 



  Verfahren zur Herstellung von orangefarbenen Küpenfarbstoffen. Behandelt man den 6-61-Diaminothioindigofarbstoff, den man aus 6-Amino-3-oxy- (I) tionaphten von der Konstitution 
 EMI1.1 
 bzw. aus der entsprechenden   Karbonsäure   durch vorsichtige Oxydation erhalten kann, mit Halogenen, so erhält man halogenhaltige neue Küpenfarbstoffe, welche Baumwolle und Wolle in sehr echten klaren orangefarbenen Tönen anfärben. Brom und Chlor liefern hierbei Farbstoffe von derselben Nuance. 



   Beispiel I. 



   10 Teile des   orangebraunen   Küpenfarbstoffes aus der genannten 6-Amino-3-oxy- (I)   thionnphten-2-Karhonsäure   werden mit etwa 100   Teilen eines Verdünnungsmittels.   z. B. 



  Chlorbonzol, Nitrobenzol, Eisessig usw.,   verrührt   und mit etwa 20 Teilen Brom versetzt ; nachdem die eingetretene Selbsterwärmung vorüber ist, erwärmt man noch einige Zeit am   Rliclnu kühler,   saugt ab, wäscht mit alkalischem Wasser und sodann mit Alkohol. 



  Das so erhaltene braune Pulver ist   untoslich in Alkohol, Aceton, schwor löslich   in heissem Nitrobenzol mit orangobrauner Farbe,   löslich   in konzentrierter Schwefelsäure mit kornblumenblauer Farbe.   t) or   Farbstoff ist je nach der angewandten Menge Brom mehr oder weniger stark bromhaltig, bei Überschüssigem   Brom   scheinen bis zu 2 Atomen Brom ein- 
 EMI1.2 
 



    In einer Suspension von 10 Teilen des orangebraunen lüpenfarbstoffes in etwa 100 Teilen 'Chlorbenzol, Nitrobenzol usw. leitet man unter Erwärmen bezw. am Rückflusskühler Chlor   ein, bis nichts mehr aufgenommen wird. Der wie im Beispiel I isolierte chlorhaltige Farb- stoff gleicht in allen Stücken dem zuvor beschriebenen bromhaltigen Farbstoff. 



   An Stelle von Brom und Chlor können auch brom-bezw. chlorliefernde Substanzen verwendet werden. 

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



   <Desc / Clms Page number 1>
 



  Process for the production of orange vat dyes. If the 6-61-diaminothioindigo dye is treated, which is obtained from 6-amino-3-oxy- (I) ionaphthene from the constitution
 EMI1.1
 or can be obtained from the corresponding carboxylic acid by careful oxidation with halogens, new vat dyes containing halogens are obtained which dye cotton and wool in very genuine, clear orange tones. Bromine and chlorine provide dyes of the same shade.



   Example I.



   10 parts of the orange-brown vat dye from said 6-amino-3-oxy- (I) thionnphten-2-carboxylic acid are mixed with about 100 parts of a diluent. z. B.



  Chlorobenzene, nitrobenzene, glacial acetic acid, etc., stirred and mixed with about 20 parts of bromine; After the self-warming that has occurred has passed, one warms the room cooler for a while, suction off, washing with alkaline water and then with alcohol.



  The brown powder thus obtained is insoluble in alcohol, acetone, swore soluble in hot nitrobenzene with an orange-brown color, soluble in concentrated sulfuric acid with a cornflower-blue color. t) or the dye contains bromine to a greater or lesser extent, depending on the amount of bromine used, with excess bromine up to 2 atoms of bromine appear
 EMI1.2
 



    In a suspension of 10 parts of the orange-brown lump dye in about 100 parts of 'chlorobenzene, nitrobenzene, etc., one passes BEZW with heating. chlorine in the reflux condenser until nothing is absorbed. The chlorine-containing dye isolated as in Example I is identical in all respects to the bromine-containing dye described above.



   Instead of bromine and chlorine, bromine or chlorine-producing substances are used.

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

 

Claims (1)

PATENT-ANSPRUCH : Verfahren zur Herstellung von orangefarbenen Küpenfarbstoffen, dadurch gekenn- zeichnet, dass man 6-Gj"Diaminothioindigo mit Halogenen behandelt. **WARNUNG** Ende CLMS Feld Kannt Anfang DESC uberlappen**. PATENT CLAIM: Process for the production of orange-colored vat dyes, characterized in that 6-Gj "diaminothioindigo is treated with halogens. ** WARNING ** End of CLMS field may overlap beginning of DESC **.
AT41780D 1907-02-13 1908-07-04 Process for the production of orange vat dyes. AT41780B (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE1907198644D DE198644C (en) 1907-02-13

Publications (1)

Publication Number Publication Date
AT41780B true AT41780B (en) 1910-04-11

Family

ID=5757087

Family Applications (1)

Application Number Title Priority Date Filing Date
AT41780D AT41780B (en) 1907-02-13 1908-07-04 Process for the production of orange vat dyes.

Country Status (1)

Country Link
AT (1) AT41780B (en)

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