CH141319A - Process for the preparation of an azine dye. - Google Patents
Process for the preparation of an azine dye.Info
- Publication number
- CH141319A CH141319A CH141319DA CH141319A CH 141319 A CH141319 A CH 141319A CH 141319D A CH141319D A CH 141319DA CH 141319 A CH141319 A CH 141319A
- Authority
- CH
- Switzerland
- Prior art keywords
- preparation
- amino
- azine dye
- sulfonic acid
- naphtophenazine
- Prior art date
Links
Description
Verfahren zur Darstellung eines Azinfar bstoffes. Wie gefunden wurde, gelangt man zu wertvollen neuen Farbstoffen der Azinreihe, wenn man 1.2-Naphtophenazinsulfosäuren in der 8-Stellung des Naphtalinkernes durch Hydroxyl oder die Amino- oder Acidyl,amino- gruppe substituiert und gegebenenfalls in den so gewonnenen 8-Amino- oder 8-Acidyl- lmino-1 .
2-naphtophenazinsulfosäuren die Sulfogruppe abspaltet und, falls nötig, die, freie Aminogruppe durch Säurereste substi tuiert.
Nach .dem vorliegenden Verfahren ge winnt man einen Farbstoff, der in gelben Nadeln kristalisiert, sich mit gelber Farbe in Wasser löst und Wolle in rötlichgelben Tönen von guter Wasch- und Walkechtheit und hervorragender Lichtechtheit färbt, in dem man 8-Amino-l.2-.naphtophenazin-5- sulfosäure mit Benzoylierungsmitteln behan delt.
Beispiel: 35 Teile Natriumsalz der 8-Amino-1 . 2- naphtophenazin-5-sulfosäure werden in 500 Teilen Wasser gelöst; naeh Zugabe von 16 'feilen Benzuyl.chlorid und 12 Teilen Na triumkarbonat wird mehrere Stunden bei 60 bis<B>70'</B> gerührt. Es kristallisiert 8-Ben- zoylamino-1 . 2-naphtophenazin-5-sulfosäure in gelben Nadeln aus.
Process for the preparation of an azine dye. As has been found, valuable new dyes of the azine series are obtained if 1,2-naphtophenazine sulfonic acids are substituted in the 8-position of the naphthalene nucleus by hydroxyl or the amino or acidyl amino group and, if appropriate, by the 8-amino or 8-amino groups obtained in this way -Acidyl-lmino-1.
2-naphtophenazinesulfonic acids split off the sulfo group and, if necessary, the free amino group is substituted by acid residues.
After .dem present process you win a dye which crystallizes in yellow needles, dissolves in water with a yellow color and dyes wool in reddish-yellow shades of good wash and milled fastness and excellent lightfastness, in which 8-amino-1.2 -.naphtophenazine-5-sulfonic acid treated with benzoylating agents.
Example: 35 parts of the sodium salt of 8-amino-1. 2- naphtophenazine-5-sulfonic acid are dissolved in 500 parts of water; After adding 16 parts of benzyl chloride and 12 parts of sodium carbonate, the mixture is stirred for several hours at 60 to 70 °. 8-Benzoylamino-1 crystallizes. 2-naphtophenazine-5-sulfonic acid in yellow needles.
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE141319X | 1928-02-07 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH141319A true CH141319A (en) | 1930-07-31 |
Family
ID=5668604
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH141319D CH141319A (en) | 1928-02-07 | 1929-01-21 | Process for the preparation of an azine dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH141319A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3165903A (en) * | 1962-03-23 | 1965-01-19 | Rateau Soc | Gas desiccation apparatus |
-
1929
- 1929-01-21 CH CH141319D patent/CH141319A/en unknown
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3165903A (en) * | 1962-03-23 | 1965-01-19 | Rateau Soc | Gas desiccation apparatus |
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