CH117477A - Process for the preparation of an alkali-like green-blue dye of the triphenylmethane series. - Google Patents
Process for the preparation of an alkali-like green-blue dye of the triphenylmethane series.Info
- Publication number
- CH117477A CH117477A CH117477DA CH117477A CH 117477 A CH117477 A CH 117477A CH 117477D A CH117477D A CH 117477DA CH 117477 A CH117477 A CH 117477A
- Authority
- CH
- Switzerland
- Prior art keywords
- blue
- green
- dye
- alkali
- preparation
- 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
- C09B11/10—Amino derivatives of triarylmethanes
- C09B11/12—Amino derivatives of triarylmethanes without any OH group bound to an aryl nucleus
- C09B11/14—Preparation from aromatic aldehydes, aromatic carboxylic acids or derivatives thereof and aromatic amines
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
Zusatzpatent zum Hauptpatent Nr. <B>116156.</B> Verfahren zur Darstellung eines alkallechten grünblauen Farbstoffes der Triphenylmetha.nreihe. Es wurde gefunden, dass man einen al- kaliechten grünblauen Farbstoff der Triphenyl- methanreihe erhält,
wenn man<B>1</B> Mol. o-Sul- fobenzaldehyd mit 2 Mol. p-Ohlorstilfobenzyl- äthylanilin kondensiert und das entstandene Kondensationsprodukt oxydiert.
Trocken ist der Farbstoff, der im Zustand der freien Säure die Di-p-chlorsulfobenzyldiä- thyldiaminoti-iphenylkarbinol-o-sLilfosäure ist, ein metallisch glänzendes blaues Pulver, das in Wasser leicht mit schöner blauer Farbe löslich ist, und färbt Wolle in blaugrünen Tönen von besonderer Reinheit undKlarheit, wobei das Färbebad ausgiebiger als bei dem entsprechenden chlorfreien Farbstoff er schöpft wird.-.
<I>Beispiel:</I> Das in bekannter Weise aus p-Chlorben- zylehlorid und Moiioäthylanilin erhaltene p-Chlorbenzyläthylaiiilin wird sul:flert, indem man<B>1</B> Teil der Base in 1-2 Teilen Schwefel- säuremonohydrat löst und in der Kälte so lange mit zwei Äquivalenten SO3 in Form von Oleum rührt, bis Alkalilöslichkeit einge treten ist.
Auf diese Weise tritt eine Sulfo- gruppe in den Benzylrest ein. Die neue Sulfosäure stellt ein weisses Pulver dar und ist in Wasser sehr schwer, in Alkalien leicht löslich.<B>65</B> Teile der Sulfosäure werden mit 23 Teilen o-Sulfobenzaldehyd (90 %ig)
in wässeriger Lösung 24 Stunden unter Rückfluss gekocht und die entstandene Leukosäure in saurer Lösung mit Bleisuperoxyd zum Farb stoff oxydiert. Nach dem Abscheiden des Bleis wird der Farbstoff ausgesalzen und getrocknet.
Additional patent to main patent no. <B> 116156. </B> Process for the preparation of an alkali-fast green-blue dye of the triphenylmethane series. It has been found that an alkaline green-blue dye of the triphenyl methane series is obtained,
if <B> 1 </B> mol. o-sulphobenzaldehyde is condensed with 2 mol. p-Ohlorstilfobenzylethylaniline and the condensation product formed is oxidized.
The dry dyestuff is di-p-chlorosulfobenzyldiä- thyldiaminoti-iphenylkarbinol-o-silfosäure in the state of the free acid, a metallic blue powder which is easily soluble in water with a beautiful blue color, and dyes wool in blue-green tones of particular purity and clarity, whereby the dye bath is exhausted more extensively than with the corresponding chlorine-free dye.
<I> Example: </I> The p-chlorobenzylethyl aniline obtained in a known manner from p-chlorobenzyl chloride and moiioethyl aniline is sul: flert by adding <B> 1 </B> part of the base in 1-2 parts of sulfur acid monohydrate and stir in the cold with two equivalents of SO3 in the form of oleum until alkali solubility has occurred.
In this way a sulfo group enters the benzyl radical. The new sulfonic acid is a white powder and is very difficult in water, easily soluble in alkalis. <B> 65 </B> parts of the sulfonic acid are mixed with 23 parts of o-sulfobenzaldehyde (90%)
Boiled under reflux in aqueous solution for 24 hours and the leuco acid formed is oxidized in acidic solution with lead peroxide to form the dye. After the lead has been deposited, the dye is salted out and dried.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH117477T | 1925-05-25 | ||
CH116156T | 1926-08-02 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH117477A true CH117477A (en) | 1926-11-01 |
Family
ID=25708652
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH117477D CH117477A (en) | 1925-05-25 | 1925-05-25 | Process for the preparation of an alkali-like green-blue dye of the triphenylmethane series. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH117477A (en) |
-
1925
- 1925-05-25 CH CH117477D patent/CH117477A/en unknown
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