CH191166A - 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
- CH191166A CH191166A CH191166DA CH191166A CH 191166 A CH191166 A CH 191166A CH 191166D A CH191166D A CH 191166DA CH 191166 A CH191166 A CH 191166A
- Authority
- CH
- Switzerland
- Prior art keywords
- dye
- preparation
- anthraquinone series
- carried out
- process according
- Prior art date
Links
Landscapes
- Coloring (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Herstellung eines Farbstoffes der Anthrachinonreihe. Gegenstand vorliegender Erfindung ist die Herstellung eines Küpenfarbstoffes durch Be handeln des Amides ans 2-Chloranthrachinoci- 3-carbonsäure und 1-lMethylamino-2-brom- anthrachinon mittels Kupfer. Die Reaktion wird zweckmässig in Gegenwart von hoch siedenden Lösungsmitteln, z.B.Chinolin,durch. geführt.
Der erhältliche Farbstoff färbt Baumwolle aus dunkelbrauner Küpe in sehr klaren und echten grünstichig gelben Tönen. Beispiel: In 400 Gewichtsteile siedendes Nitro- benzol trägt man ein Gemisch von 60 Ge wichtsteilen Kupferpulver und 60 Gewichts teilen der Acylverbindung folgender Struktur ein
EMI0001.0016
Nach etwa 12stündigem Sieden wird das Reaktionsprodukt zwecks Entfernung des Kupfers mit warmer, verdünnter Salpetersäure behandelt. Der Rückstand wird aus viel Chino- lin oder Nitrobenzol umkristallisiert.
Der er haltene Farbstoff ist halogenfrei und unver- seifbar. Er färbt Baumwolle aus brauner Küpe in klaren grünstichig gelben Tönen von guten Echtheitseizenschaften an.
Process for the preparation of a dye of the anthraquinone series. The present invention relates to the production of a vat dye by treating the amide of 2-chloroanthraquinoci-3-carboxylic acid and 1-methylamino-2-bromo-anthraquinone using copper. The reaction is best carried out in the presence of high-boiling solvents, e.g. quinoline. guided.
The available dye dyes cotton from a dark brown vat in very clear and genuine greenish yellow tones. Example: A mixture of 60 parts by weight of copper powder and 60 parts by weight of the acyl compound of the following structure is added to 400 parts by weight of boiling nitrobenzene
EMI0001.0016
After boiling for about 12 hours, the reaction product is treated with warm, dilute nitric acid to remove the copper. The residue is recrystallized from a large amount of quinoline or nitrobenzene.
The dye obtained is halogen-free and unsaponifiable. It dyes cotton from a brown vat in clear greenish yellow shades with good fastness properties.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE191166X | 1934-12-29 | ||
CH188322T | 1935-12-28 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH191166A true CH191166A (en) | 1937-05-31 |
Family
ID=25721631
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH191166D CH191166A (en) | 1934-12-29 | 1935-12-28 | Process for the preparation of a dye of the anthraquinone series. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH191166A (en) |
-
1935
- 1935-12-28 CH CH191166D patent/CH191166A/en unknown
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