CH101757A - Process for the preparation of a vat dye. - Google Patents
Process for the preparation of a vat dye.Info
- Publication number
- CH101757A CH101757A CH101757DA CH101757A CH 101757 A CH101757 A CH 101757A CH 101757D A CH101757D A CH 101757DA CH 101757 A CH101757 A CH 101757A
- Authority
- CH
- Switzerland
- Prior art keywords
- dye
- preparation
- red
- vat dye
- vat
- 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
- C09B5/00—Dyes with an anthracene nucleus condensed with one or more heterocyclic rings with or without carbocyclic rings
- C09B5/62—Cyclic imides or amidines of peri-dicarboxylic acids of the anthracene, benzanthrene, or perylene series
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Darstellung eines Nüpenfarbstoffes. Es ist gefunden worden, dass man durch Kondensation von Perylen-3.4.9.10-tetra- carbonsä ure mit p-Chloranilin einen wert vollen Küpenfarbstoff erhält.
<I>Beispiel:</I> 392 Gewichtsteile Perylentetracarbon- säureanhydricl werden mit etwa 3500 Ge wichtsteilen p-Chloranilin un.;er Rühren auf etwa 190 bis 200' bis zum Verschwinden des Perylentetracarbonsäureanhydrids erhitzt. Nach beendeter Farbstoffbildung lässt man auf etwa 80 abkühlen, rührt etwa 5000 Ge wichtsteile Alkohol ein und filtriert den ab geschiedenen Farbstoff ab.
Er wird mit Alkohol ausgewaschen und schliesslich, zur Entfernung geringer alkalilöslicher Verun reinigungen mit verdünnter, heisser Kali lauge ausgezogen. Die Ausbeute ist fast quantitativ.
Der in braunroten Kristallnadeln er haltene Farbstoff wird von konzentrierter Schwefelsäure violett gelöst. Die gebräuch lichen organischen Lösungsmittel nehmen nur wenig mit gelbgrüner Fluoreszenz auf. Die Hydrosulfitküpe ist rotviolett. Baum wolle wird daraus in echten roten Tönen angefärbt.
Process for the preparation of a pebble dye. It has been found that a valuable vat dye is obtained by condensing perylene-3.4.9.10-tetra-carboxylic acid with p-chloroaniline.
<I> Example: </I> 392 parts by weight of perylenetetracarboxylic acid anhydride are heated with about 3500 parts by weight of p-chloroaniline and stirring to about 190 to 200 'until the perylenetetracarboxylic acid anhydride has disappeared. After the formation of the dye has ended, the mixture is allowed to cool to about 80, about 5000 parts by weight of alcohol are stirred in and the dyestuff which has separated off is filtered off.
It is washed out with alcohol and finally, to remove minor alkali-soluble impurities, it is stripped with diluted, hot potash lye. The yield is almost quantitative.
The dye, contained in red-brown crystal needles, is dissolved in a violet color by concentrated sulfuric acid. The common organic solvents absorb little with yellow-green fluorescence. The hydrosulfite vat is red-violet. It is used to dye cotton in real red tones.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH100706T | 1923-01-03 | ||
CH101757T | 1923-01-03 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH101757A true CH101757A (en) | 1923-10-16 |
Family
ID=25705880
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH101757D CH101757A (en) | 1923-01-03 | 1923-01-03 | Process for the preparation of a vat dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH101757A (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2543747A (en) * | 1948-08-27 | 1951-03-06 | Gen Aniline & Film Corp | Preparation of n.n'-diaryl derivatives of perylene diimid |
DE1031449B (en) * | 1955-06-13 | 1958-06-04 | Bayer Ag | Process for the production of Kuepen dyes |
DE1067548B (en) * | 1956-05-18 | 1959-10-22 | Hoechst Ag | Process for the preparation of a dye |
DE1067952B (en) * | 1959-10-29 | Farbwerke Hoechst Aktiengesellschaft vormals Meister Lucius & Bruning, Frankfurt/M | Process for the preparation of a dye | |
DE1105085B (en) * | 1958-12-13 | 1961-04-20 | Hoechst Ag | Process for the preparation of a dye |
DE1105084B (en) * | 1958-12-13 | 1961-04-20 | Hoechst Ag | Process for the preparation of a dye |
-
1923
- 1923-01-03 CH CH101757D patent/CH101757A/en unknown
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1067952B (en) * | 1959-10-29 | Farbwerke Hoechst Aktiengesellschaft vormals Meister Lucius & Bruning, Frankfurt/M | Process for the preparation of a dye | |
US2543747A (en) * | 1948-08-27 | 1951-03-06 | Gen Aniline & Film Corp | Preparation of n.n'-diaryl derivatives of perylene diimid |
DE1031449B (en) * | 1955-06-13 | 1958-06-04 | Bayer Ag | Process for the production of Kuepen dyes |
DE1067548B (en) * | 1956-05-18 | 1959-10-22 | Hoechst Ag | Process for the preparation of a dye |
DE1105085B (en) * | 1958-12-13 | 1961-04-20 | Hoechst Ag | Process for the preparation of a dye |
DE1105084B (en) * | 1958-12-13 | 1961-04-20 | Hoechst Ag | Process for the preparation of a dye |
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