CH192490A - Process for the preparation of a dye of the anthraquinone series. - Google Patents
Process for the preparation of a dye of the anthraquinone series.Info
- Publication number
- CH192490A CH192490A CH192490DA CH192490A CH 192490 A CH192490 A CH 192490A CH 192490D A CH192490D A CH 192490DA CH 192490 A CH192490 A CH 192490A
- Authority
- CH
- Switzerland
- Prior art keywords
- dye
- preparation
- anthraquinone series
- parts
- weight
- Prior art date
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- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Coloring (AREA)
Description
Verfahren zur Darstellung eines Farbstoffes der Anthrachinonreihe. Gegenstand dieses Zusatzpatentes ist ein Verfahren zur Darstellung eines Farbstoffes der Anthrachinonreihe, welches dadurch ge kennzeichnet ist, dass man 1-Bromanthrachi- non-2-sulfochlorid mit Methyltaurin konden siert und das so erhaltene 1-Bromanthra- chinon-2-sulfomethyltaurid weiter mit m-Ami- nodimethylanilin kondensiert.
<I>Beispiel:</I> 270 Gewichtsteile 1-Bromantbrachinon-2- sulfochlorid, 110 Gewichtsteile Methyltaurin, 80 Gewichtsteile Soda calc. werden in 2000 Teilen Wasser 5 Stunden bei<B>80-850</B> ge rührt. Die erhaltene Lösung wird heiss filtriert und erkalten gelassen, wobei sich das Na triumsalz des 1-Bromanthrachinon-2-sulfo- methyltaurid ausscheidet. Man saugt ab und wäscht mit 10o/oiger Kochsalzlösung neutral.
25 Gewichtsteile des so erhaltenen 1- Bromanthrachinon-2-sulfomethyltaurid (Na- Salz), 20 Gewichtsteile m-Aminodimethyl- anilin, 5 Gewichtsteile calc. Soda, 250 Ge wichtsteile Wasser und 0,5 Gewichtsteile Kupferchlorür werden solange bei 40-50 o C gerührt, bis die Kondensation beendet ist.
Nach Aufarbeitung des Reaktionsgemisches erhält man einen grünen, kristallinischen Farbstoff, der sich in Wasser mit klarer grüner Farbe löst und auf Wolle klare gelb atichiggrüne Farbtöne liefert.
Process for the preparation of a dye of the anthraquinone series. The subject of this additional patent is a process for the preparation of a dye of the anthraquinone series, which is characterized in that 1-bromoanthraquinone-2-sulfochloride is condensed with methyltaurine and the 1-bromoanthraquinone-2-sulfomethyltauride obtained in this way continues with m - Ami- nodimethylaniline condensed.
<I> Example: </I> 270 parts by weight of 1-bromantbrachinone-2-sulfochloride, 110 parts by weight of methyl taurine, 80 parts by weight of soda calc. are stirred in 2000 parts of water at <B> 80-850 </B> for 5 hours. The resulting solution is filtered hot and allowed to cool, the sodium salt of 1-bromoanthraquinone-2-sulfomethyltauride separating out. It is suctioned off and washed neutral with 10% sodium chloride solution.
25 parts by weight of the 1-bromoanthraquinone-2-sulfomethyl tauride (Na salt) obtained in this way, 20 parts by weight of m-aminodimethyl aniline, 5 parts by weight of calc. Soda, 250 parts by weight of water and 0.5 parts by weight of copper chloride are stirred at 40-50 o C until the condensation has ended.
After working up the reaction mixture, a green, crystalline dye is obtained which dissolves in water with a clear green color and gives clear, yellowish green color shades on wool.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE192490X | 1935-03-01 | ||
CH189872T | 1936-02-27 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH192490A true CH192490A (en) | 1937-08-15 |
Family
ID=25721899
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH192490D CH192490A (en) | 1935-03-01 | 1936-02-27 | Process for the preparation of a dye of the anthraquinone series. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH192490A (en) |
-
1936
- 1936-02-27 CH CH192490D patent/CH192490A/en unknown
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