CH261278A - Process for the production of a new dye of the anthraquinone series. - Google Patents
Process for the production of a new dye of the anthraquinone series.Info
- Publication number
- CH261278A CH261278A CH261278DA CH261278A CH 261278 A CH261278 A CH 261278A CH 261278D A CH261278D A CH 261278DA CH 261278 A CH261278 A CH 261278A
- Authority
- CH
- Switzerland
- Prior art keywords
- production
- anthraquinone series
- new dye
- dye
- sulfuric acid
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B1/00—Dyes with anthracene nucleus not condensed with any other ring
- C09B1/16—Amino-anthraquinones
- C09B1/20—Preparation from starting materials already containing the anthracene nucleus
- C09B1/22—Dyes with unsubstituted amino groups
- C09B1/24—Dyes with unsubstituted amino groups sulfonated
Description
Zusatzpatent zum Hauptpatent Nr. 253955. Verfahren zur Herstellung eines neuen Farbstoffes der Anthrachinonreihe. Das vorliegende Patent betrifft ein Ver fahren zur Herstellung eines neuen Farb stoffes der Anthrachinonreihe und ist da durch gekennzeichnet, dass man 1-Amino-4- brom - 6,7 - dichloranthrachinon-2-sulfonsäure mit p-Toluolsulfamid kondensiert und das Kondensationsprodukt hernach verseift.
<I>Beispiel:</I> 30 Gewichtsteile 1-Amino-4-brom-6,7-di- chloranthrachinon-2-sulfonsäure werden mit 18 Gewichtsteilen p-Toluolsulfamid, 8,8 Ge wichtsteilen Natriumbicarbonat und 0,5 Ge wichtsteilen Kupferchlorür in 350 Teilen Wasser unter Rühren während 2 Stunden auf 70 und 2 Stunden auf 80 erhitzt.
Nach erfolgter Kondensation wird das Reaktionsprodukt auf übliche Weise aufgear beitet und durch Digerieren in konzentrierter Schwefelsäure bei gewöhnlicher oder erhöhter Temperatur verseift. Durch Ausladen in ein Wasser-Eis-Gemisch gewinnt man die 1,4-Di- amino-6,7-dichloranthrachinon-2-sulfonsäure.
Man erhält sie auch durch Zusatz von wenig Wasser zur schwefelsauren Lösung, worauf ihr schwefelsaures Salz ausfällt, das auf übliche Weise in die Säure übergeführt werden kann.
Der Farbstoff löst sich in konzentrierter Schwefelsäure mit hellgelber Farbe, die beim Zusatz von wenig Paraformaldehyd in Blau umschlägt. Er färbt tierische Fasern, z. B. Wolle, Seide, und künstliche Fasern wie Nylon in rotstickig violetten Tönen von guten Echtheiten.
Additional patent to main patent No. 253955. Process for the production of a new dye of the anthraquinone series. The present patent relates to a process for the production of a new dye of the anthraquinone series and is characterized by the fact that 1-amino-4-bromo-6,7-dichloroanthraquinone-2-sulfonic acid is condensed with p-toluenesulfamide and the condensation product is saponified afterwards .
<I> Example: </I> 30 parts by weight of 1-amino-4-bromo-6,7-dichloranthraquinone-2-sulfonic acid are mixed with 18 parts by weight of p-toluenesulfamide, 8.8 parts by weight of sodium bicarbonate and 0.5 parts by weight Copper chloride in 350 parts of water is heated to 70 and 2 hours to 80 for 2 hours with stirring.
After condensation has taken place, the reaction product is worked up in the usual way and saponified by digestion in concentrated sulfuric acid at normal or elevated temperature. The 1,4-di-amino-6,7-dichloroanthraquinone-2-sulfonic acid is obtained by unloading into a water-ice mixture.
They are also obtained by adding a little water to the sulfuric acid solution, whereupon their sulfuric acid salt precipitates, which can be converted into the acid in the usual way.
The dye dissolves in concentrated sulfuric acid with a light yellow color, which turns blue when a little paraformaldehyde is added. It dyes animal fibers, e.g. B. wool, silk, and artificial fibers such as nylon in red-embroidered violet shades of good fastness properties.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH261278T | 1946-10-10 | ||
CH253955T | 1948-04-15 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH261278A true CH261278A (en) | 1949-04-30 |
Family
ID=25729811
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH261278D CH261278A (en) | 1946-10-10 | 1946-10-10 | Process for the production of a new dye of the anthraquinone series. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH261278A (en) |
-
1946
- 1946-10-10 CH CH261278D patent/CH261278A/en unknown
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