CH224549A - Process for the preparation of a new dye of the anthraquinone series. - Google Patents
Process for the preparation of a new dye of the anthraquinone series.Info
- Publication number
- CH224549A CH224549A CH224549DA CH224549A CH 224549 A CH224549 A CH 224549A CH 224549D A CH224549D A CH 224549DA CH 224549 A CH224549 A CH 224549A
- Authority
- CH
- Switzerland
- Prior art keywords
- preparation
- new dye
- anthraquinone series
- parts
- bromo
- Prior art date
Links
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- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Coloring (AREA)
Description
Verfahren zur Darstellung eines neuen Farbstoffes der Anthraehinonreihe. Das vorliegende Patent betrifft ein Ver fahren zur Darstellung eines neuen Farb stoffes der Anthrachinonreihe und ist da durch gekennzeichnet, dass man 1-Amino-2- brom-4-(2', 4'-dimethyl)-phenylamino-6-chlor- anthrachinon mit Brom behandelt und die erhaltene bromierte Verbindung sulfiert. <I>Beispiel:
</I> 14 Teile 1 - Amino - 2 - brom-4- (2',4'-di- methyl) - phenylamino - 6 - chloranthrachinon (dargestellt durch Dibromierung von 1- Amino-6-monochloranthrachinon und nach folgende Kondensation mit m-Xylidin) wer den in 150 Teilen Dichlorbenzol verrührt und mit 5,2 Teilen Brom, gelöst in 20 Teilen Dichlorbenzol,
versetzt. Man lässt einige Zeit bei Raumtemperatur rühren und erwärmt dann kurze Zeit auf dem Wasserbade. Die erhaltene Base, das 1-Amino-2-brom-4-(2',4' dimethyl-6'-brom)-phenylamino-6-monochlor- anthrachinon wird durch Abblasen des Lö sungsmittels und Filtration abgetrennt und getrocknet.
10 Teile der erhaltenen Base werden mit 40 Teilen Phenol und 20 Teilen 30%iger Wässeriger galiumsulfitlösung 16 Stunden im Autoklaven auf 140 erhitzt. Das Phenol wird sodann abgeblasen und der Farbstoff abgetrennt. Er besitzt die Formel
EMI0001.0041
und färbt Wolle in lebhaften blauen Tönen von guten Echtheiten.
Process for the preparation of a new dye of the anthraehinone series. The present patent relates to a process for the preparation of a new dye of the anthraquinone series and is characterized by the fact that 1-amino-2-bromo-4- (2 ', 4'-dimethyl) phenylamino-6-chloro-anthraquinone treated with bromine and sulfated the brominated compound obtained. <I> example:
</I> 14 parts of 1 - amino - 2 - bromo-4- (2 ', 4'-dimethyl) - phenylamino - 6 - chloranthraquinone (prepared by dibromination of 1-amino-6-monochloranthraquinone and after the subsequent condensation with m-xylidine) who is stirred in 150 parts of dichlorobenzene and treated with 5.2 parts of bromine dissolved in 20 parts of dichlorobenzene,
offset. The mixture is left to stir for some time at room temperature and then warmed for a short time on the water bath. The base obtained, the 1-amino-2-bromo-4- (2 ', 4' dimethyl-6'-bromo) -phenylamino-6-monochloro-anthraquinone, is separated off by blowing off the solvent and filtration and dried.
10 parts of the base obtained are heated to 140 for 16 hours in an autoclave with 40 parts of phenol and 20 parts of 30% strength aqueous galium sulfite solution. The phenol is then blown off and the dye separated. He owns the formula
EMI0001.0041
and dyes wool in vivid blue tones with good fastness properties.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH224549T | 1940-12-13 | ||
CH219415T | 1940-12-13 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH224549A true CH224549A (en) | 1942-11-30 |
Family
ID=25726271
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH224549D CH224549A (en) | 1940-12-13 | 1940-12-13 | Process for the preparation of a new dye of the anthraquinone series. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH224549A (en) |
-
1940
- 1940-12-13 CH CH224549D patent/CH224549A/en unknown
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