CH203051A - 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
- CH203051A CH203051A CH203051DA CH203051A CH 203051 A CH203051 A CH 203051A CH 203051D A CH203051D A CH 203051DA CH 203051 A CH203051 A CH 203051A
- Authority
- CH
- Switzerland
- Prior art keywords
- dye
- preparation
- chromable
- anhydride
- 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
- C09B11/10—Amino derivatives of triarylmethanes
- C09B11/24—Phthaleins containing amino groups ; Phthalanes; Fluoranes; Phthalides; Rhodamine dyes; Phthaleins having heterocyclic aryl rings; Lactone or lactame forms of triarylmethane dyes
- C09B11/245—Phthaleins having both OH and amino substituent(s) on aryl ring
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Coloring (AREA)
Description
<B>Zusatzpatent</B> zum Hauptpatent Nr. 198713. Verfahren zur Darstellung eines ehromierbaren Farbstoffes der Triarylmethanreihe. Gegenstand dieses Zusatzpatentes ist ein Verfahren zur Darstellung eines ehromier- baren Farbstoffes der Triarylmethanreihe, welches dadurch gekennzeichnet ist, dass man m-Diäthylaminophenol mit 3-Oxytrimellith- sänlre-anhydrid kondensiert.
<I>Beispiel:</I> 4,2 Gewichtsteile 3-Ogytrimellithsäure- anhydrid:
EMI0001.0015
(darstellbar durch Bromieren von Pseudo- cumol-5:sulfosäuTe in konzentriertet 18chwe- felsäure, Abspalten der @Sulfogruppe, Oxy dation und Ersatz des Bromatoms gegen die Hydroxylgruppe) und 2,2 Gewichtsteile m-Diäthyl:amiuophenol werden zirka drei 'Sunden bei 1180-190C C unter Rühren ver schmolzen.
Nach beendeter Reaktion lässt man erkalten. Die pulverisierte Schmelze wird mit konzentrierter :Salzsäure kalt ver- rühTt, wobei der Farbstoff in Lösung geht. Man saugt vom Rückstand (unveränderte 3-Oxytrimellithsäure) ab und fällt,den Farb stoff aus dem salzsauren Filtrat mit Wasser aus.
Der abgesaugte Farbstoff wird in Bi- carbonat oder )Sodalösung gelöst und zur Trockne eingedampft.
Er färbt -aus saurem Bade die tierische Faser in sehr klaren blaustichig roten Tönen, welche nachchromiert noch etwas blau stichiger werden und dann sehr ,gute Echt- heitseigenscUaften besitzen.
<B> Additional patent </B> to the main patent No. 198713. Process for the preparation of an honorable dye of the triarylmethane series. The subject of this additional patent is a process for the preparation of an honorable dye of the triarylmethane series, which is characterized in that m-diethylaminophenol is condensed with 3-oxytrimellitic acid anhydride.
<I> Example: </I> 4.2 parts by weight 3-ogytrimellitic anhydride:
EMI0001.0015
(Can be prepared by brominating pseudo-cumol-5: sulfo acid in concentrated 18-sulfuric acid, splitting off the @sulfo group, oxidizing and replacing the bromine atom with the hydroxyl group) and 2.2 parts by weight of m-diethyl: amiuophenol are about three hours at 1180 -190C C melted while stirring.
After the reaction has ended, it is allowed to cool. The pulverized melt is stirred cold with concentrated hydrochloric acid, whereby the dye goes into solution. The residue (unchanged 3-oxytrimellitic acid) is filtered off with suction and the dye is precipitated from the hydrochloric acid filtrate with water.
The sucked off dye is dissolved in bicarbonate or soda solution and evaporated to dryness.
It dyes the animal fibers from an acid bath in very clear blue-tinged red tones, which, when chromed, become a little blue-tinged and then have very, good fastness properties.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE203051X | 1936-02-26 | ||
CH198713T | 1938-12-20 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH203051A true CH203051A (en) | 1939-02-15 |
Family
ID=25723136
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH203051D CH203051A (en) | 1936-02-26 | 1937-02-18 | Process for the preparation of a chromable dye of the triarylmethane series. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH203051A (en) |
-
1937
- 1937-02-18 CH CH203051D patent/CH203051A/en unknown
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CH203051A (en) | Process for the preparation of a chromable dye of the triarylmethane series. | |
CH203047A (en) | Process for the preparation of a chromable dye of the triarylmethane series. | |
CH191753A (en) | Process for the preparation of an acidic chromating dye of the anthraquinone series. | |
CH132905A (en) | Procedure for the representation of 1. 2-Benzanthraquinone-peri-dicarboxylic acid anhydride. | |
CH178422A (en) | Process for the production of a nitrogen-containing condensation product. | |
CH170768A (en) | Process for the preparation of a substantive copper-containing azo dye. | |
CH192481A (en) | Process for the production of a new pyrene derivative. | |
CH203049A (en) | Process for the preparation of a chromable dye of the triarylmethane series. | |
CH203053A (en) | Process for the preparation of a chromable dye of the triarylmethane series. | |
CH120257A (en) | Process for the preparation of a new oxynaphthalene carboxylic acid. | |
CH185588A (en) | Process for the preparation of an acidic dye of the anthraquinone series. | |
CH148355A (en) | Process for the preparation of an m-oxy-phenylarylamine carboxylic acid. | |
CH175885A (en) | Process for the preparation of a substantive copper-containing azo dye. | |
CH203054A (en) | Process for the preparation of a chromable dye of the triarylmethane series. | |
CH194657A (en) | Process for the preparation of 4-nitro-2-amino-1-oxynaphthalene-7-sulfonic acid. | |
CH203057A (en) | Process for the preparation of a chromable dye of the triarylmethane series. | |
CH175881A (en) | Process for the preparation of a substantive copper-containing azo dye. | |
CH171232A (en) | Process for the production of a new azo dye. | |
CH178109A (en) | Process for the production of a new azo dye. | |
CH175882A (en) | Process for the preparation of a substantive copper-containing azo dye. | |
CH177851A (en) | Process for the preparation of a lightfast dye of the quinoline series. | |
CH203045A (en) | Process for the preparation of a chromable dye of the triarylmethane series. | |
CH203050A (en) | Process for the preparation of a chromable dye of the triarylmethane series. | |
CH198611A (en) | Process for the production of a sulfur dye. | |
CH145328A (en) | Process for the preparation of an azophthalein dye. |