CH211436A - Process for the preparation of a chromable dye of the triarylmethane series. - Google Patents
Process for the preparation of a chromable dye of the triarylmethane series.Info
- Publication number
- CH211436A CH211436A CH211436DA CH211436A CH 211436 A CH211436 A CH 211436A CH 211436D A CH211436D A CH 211436DA CH 211436 A CH211436 A CH 211436A
- Authority
- CH
- Switzerland
- Prior art keywords
- dye
- chromable
- preparation
- bromine
- triarylmethane series
- 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
- C09B11/00—Diaryl- or thriarylmethane dyes
- C09B11/04—Diaryl- or thriarylmethane dyes derived from triarylmethanes, i.e. central C-atom is substituted by amino, cyano, alkyl
- C09B11/06—Hydroxy derivatives of triarylmethanes in which at least one OH group is bound to an aryl nucleus and their ethers or esters
- C09B11/08—Phthaleins; Phenolphthaleins; Fluorescein
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
Zusatzpatent zum Hauptpatent Nr. 198713. Verfahren zur Herstellung eines ehr omierbaren Farbstoffes der Triarylmethanr eihe. Gegenstand dieses Zusatzpatentes ist ein Verfahren zur Herstellung eines chromier- baren Farbstoffes der Triarylmethanreihe, welches dadurch gekennzeichnet ist,
dass man 1 Mol 5-Ogytrimellitsäureanhydrid mit 2 Mol ss-Resorcylsäure kondensiert und 1 Mol des so erhaltenen Farbstoffes mit etwa 4 Mol Brom behandelt.
<I>Beispiel:</I> 21 Gewichtsteile 5-Ogytrimellitsäureanhy- drid, 31 Gewichtsteile ss-Resorcylsäure, 14 Gewichtsteile wasserfreies Chlorzink werden verrieben und im Ölbad mehrere Stunden bis zum Festwerden der Schmelze auf<B>1.80'</B> C erhitzt. Nach dem Abkühlen wird pulveri siert und mit 200 Gewichtsteilen 5%iger Salzsäure ausgekocht, und der gelbe Rück stand warm abgesaugt. Man löst diesen Farbstoff in verdünnter Sodalösung, worin er mit orangeroter Farbe und grüner Fluor eszenz löslich ist, filtriert und fällt den Farbstoff mit verdünnten Säuren wieder aus.
Zur weiteren Reinigung kann er aus wäss- rigem Alkohol umgelöst werden.
40 Gewichtsteile dieses Farbstoffes wer den in<B>160</B> Gewichtsteilen Alkohol suspen diert und bei gewöhnlicher Temperatur lang sam unter Rühren mit 64 Gewichtsteilen Brom versetzt. Nach mehrstündigem Stehen wird mit dem doppelten Volumen Wasser verdünnt, der ausfallende rote Farbstoff ab gesaugt, kongoneutral gewaschen und durch Lösen in Bicarbonatlösung und Eindampfen in das Natriumsalz übergeführt. Der Farb stoff färbt die tierische Faser aus saurem Bade in sehr klaren, gelbstichig roten Tö nen, deren Echtheitseigenschaften durch Nachchromieren verbessert werden.
Additional patent to the main patent No. 198713. Process for the production of an honorable dye of the triarylmethane series. The subject of this additional patent is a process for the production of a chromable dye of the triarylmethane series, which is characterized by
that 1 mol of 5-ogytrimellitic anhydride is condensed with 2 mol of β-resorcylic acid and 1 mol of the dye thus obtained is treated with about 4 mol of bromine.
<I> Example: </I> 21 parts by weight of 5-ogytrimellitic anhydride, 31 parts by weight of β-resorcylic acid, 14 parts by weight of anhydrous zinc chloride are rubbed in and in an oil bath for several hours until the melt solidifies at 1.80 ° C heated. After cooling, it is pulverized and boiled with 200 parts by weight of 5% hydrochloric acid, and the yellow residue was sucked off warm. This dye is dissolved in dilute soda solution, in which it is soluble with an orange-red color and green fluorescence, filtered and the dye is precipitated again with dilute acids.
For further cleaning it can be redissolved from aqueous alcohol.
40 parts by weight of this dye are suspended in 160 parts by weight of alcohol and 64 parts by weight of bromine are slowly added at ordinary temperature while stirring. After standing for several hours, the mixture is diluted with twice the volume of water, the red dye which has precipitated is sucked off, washed in a Congo-neutral manner and converted into the sodium salt by dissolving it in bicarbonate solution and evaporation. The dye colors the animal fibers from acid baths in very clear, yellowish red tones, the fastness properties of which are improved by re-chrome plating.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH211436T | 1937-03-25 | ||
CH198713T | 1938-12-20 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH211436A true CH211436A (en) | 1940-09-15 |
Family
ID=25723127
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH211436D CH211436A (en) | 1937-03-25 | 1937-03-25 | Process for the preparation of a chromable dye of the triarylmethane series. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH211436A (en) |
-
1937
- 1937-03-25 CH CH211436D patent/CH211436A/en unknown
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