CH117479A - 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
- CH117479A CH117479A CH117479DA CH117479A CH 117479 A CH117479 A CH 117479A CH 117479D A CH117479D A CH 117479DA CH 117479 A CH117479 A CH 117479A
- 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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Zusatzpatent zum Hauptpatent Nr. <B>116156.</B> Verfahren zur Darstellung eines alkaliechten grünblauen Farbstoffes der Triphenylmethanreihe. Es wurde gefunden, 'dass man einen alka- liechten grünblauen Farbstoff der Triphenyl- methanreihe erhält,
wenn man<B>1</B> Mol. o-Sulfo- benzaldehyd mit 2 Mol. 2.4-Dichloi-sulfo- benzyläthylanilin kondensiert und das ent standene Kondensationsprodukt oxydiert.
Trocken istderFarbstoff, derimZustand der freien Säure die Di-2.4-dichlorsulfobenzyl- diäthyldiaininotriphenylkarbinol <B>-</B> o<B>-</B> sulfogätire 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 und Klarheit, wobei das Färbebad ausgiebiger als bei dem entsprechenden chlorfreien Farbstoff erschöpft wird.
Reispiel.- Das in bekannter Weise aus 2.4-Dichlor- benzylchlorid und Monoäthylanilin erhaltene 2.4-Dichlorbenzyläthylanilin wird sulflert, in dem man<B>1</B> Teil der Base in 1-2 Teilen Schwefelsäuremonohydrat löst und in der<B>Käl</B>te solange 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 Stilfo- säure stellt ein weisses Pulver dar und ist in Wasser sehr schwer, in Alkalien leicht löslich. <B>72</B> Teile der Sulfosäure werden mit<B>23</B> Teilen o-Sulfobenzyldehyd <B>(90</B> II/o ig) in wässriger Lösung 24 Stunden unter Rückfluss gekocht und die entstandene Leukosäure in saurer Lösung mit Bleisuperoxyd zum Farbstoff oxy diert.
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-proof green-blue dye of the triphenylmethane series. It has been found that an alkali-like green-blue dye of the triphenyl methane series is obtained,
if <B> 1 </B> mol. o-sulfobenzaldehyde is condensed with 2 mol. 2,4-dichloisulfobenzylethylaniline and the condensation product formed is oxidized.
The dry color is the di-2,4-dichlorosulfobenzyl diethyldiaininotriphenylcarbinol in the free acid state, a metallic, shiny blue powder that is easily soluble in water with a beautiful blue color is, and dyes wool in blue-green shades of particular purity and clarity, whereby the dye bath is exhausted more extensively than with the corresponding chlorine-free dye.
Rebeispiel.- The 2,4-dichlorobenzylethylaniline obtained in a known manner from 2,4-dichlorobenzyl chloride and monoethylaniline is sulphurized by dissolving 1 part of the base in 1-2 parts of sulfuric acid monohydrate and adding to the cal </B> te as long as stirred 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 stilfic acid is a white powder and is very difficult in water and easily soluble in alkalis. <B> 72 </B> parts of the sulfonic acid are refluxed with <B> 23 </B> parts of o-sulfobenzyldehyde (90 </B> II / o ig) in aqueous solution for 24 hours and the resulting Leucosic acid in acidic solution is oxidized 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 |
---|---|---|---|
CH117479T | 1925-05-25 | ||
CH116156T | 1926-08-02 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH117479A true CH117479A (en) | 1926-11-01 |
Family
ID=25708654
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH117479D CH117479A (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) | CH117479A (en) |
-
1925
- 1925-05-25 CH CH117479D patent/CH117479A/en unknown
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