CH294951A - Process for the production of a vat dye. - Google Patents
Process for the production of a vat dye.Info
- Publication number
- CH294951A CH294951A CH294951DA CH294951A CH 294951 A CH294951 A CH 294951A CH 294951D A CH294951D A CH 294951DA CH 294951 A CH294951 A CH 294951A
- Authority
- CH
- Switzerland
- Prior art keywords
- production
- vat
- chloro
- dye
- vat dye
- 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
- C09B1/00—Dyes with anthracene nucleus not condensed with any other ring
- C09B1/16—Amino-anthraquinones
- C09B1/20—Preparation from starting materials already containing the anthracene nucleus
- C09B1/36—Dyes with acylated amino groups
- C09B1/42—Dyes with acylated amino groups the acyl groups being residues of an aromatic carboxylic acid
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
<B>Zusatzpatent</B> zum Hauptpatent Nr. 289992. Verfahren zur Herstellung <B>eines</B> Küpenfarbstoffes. Es wurde gefunden, dass man zu einem wertvollen Küpenfarbstoff gelangt, wenn man zwei Verbindungen der Formeln
EMI0001.0008
worin das eine X eine NH2-Gruppe und das andere X ein Halogenatom bedeutet, mitein ander kondensiert.
Der neue Farbstoff löst sich in konzen trierter Schwefelsäure mit braunoranger Farbe und färbt Baumwolle aus bordeauxroter Küpe in reinen grünstichig gelben Tönen.
Beim vorliegenden Verfahren kann man entweder ein 1-Halogen-6-fluoranthrachinon, vorzugsweise 1-Chlor-6-fluoranthraehinon,oder 1-Amino-6-fluoranthrachinon als den einen Ausgangsstoff verwenden. Als zweiter Aus gangsstoff kommt 4'-Chlor-1,1'-diphenyl.-4- earbonsäureamid oder ein 4'-Chlor-1,1'-diphe- nyl-4-carbonsäurehalogenid, insbesondere das Chlorid dieser Säure in Betracht.
Die gemäss vorliegendem Verfahren aus zuführenden Kondensationen erfolgen zweck mässig in einem hochsiedenden organischen Lösungsmittel wie Nitrobenzol oder o-Dichlor- benzol und bei erhöhter Temperatur. Bei der Kondensation der 1-Halogen-6-fluoranthra.. chinone mit dem 4'-Chlor-diphenylcarbon- säureamid empfiehlt es sich, dem Reaktions gemisch ein säurebindendes Mittel, z. B. Na trium- oder Kaliumcarbonat, und ausserdem ein Kupfersalz wie Kupfer(I)acetat oder Kupfer (I) bromid zuzufügen.
<I>Beispiel:</I> 12 Teile 1.-Amino-6-fluoranthrachinon und 7.4 Teile 4'-Chlor-1,1'-diphenyl-4-carbonsäure- chlorid werden 2 Stunden bei 125 bis 130 verrührt.. Nach dem Erkalten wird der in gelben Nadeln ausgefallene Farbstoff abge saugt, mit Nitrobenzol und kochendem Alko hol gewaschen und getrocknet.
<B> Additional patent </B> to main patent no. 289992. Process for the production of <B> a </B> vat dye. It has been found that a valuable vat dye is obtained by using two compounds of the formulas
EMI0001.0008
wherein one X is an NH2 group and the other X is a halogen atom, condensed with one another.
The new dye dissolves in concentrated sulfuric acid with a brown-orange color and dyes cotton from a burgundy vat in pure greenish yellow tones.
In the present process, either a 1-halo-6-fluoroanthraquinone, preferably 1-chloro-6-fluoroanthraquinone, or 1-amino-6-fluoroanthraquinone can be used as the one starting material. A second starting material is 4'-chloro-1,1'-diphenyl.-4-carboxamide or a 4'-chloro-1,1'-diphenyl-4-carboxylic acid halide, in particular the chloride of this acid.
The condensations fed in according to the present process are expediently carried out in a high-boiling organic solvent such as nitrobenzene or o-dichlorobenzene and at elevated temperature. In the condensation of the 1-halogen-6-fluoroanthra .. quinones with the 4'-chloro-diphenylcarboxylic acid amide, it is advisable to add an acid-binding agent to the reaction mixture, eg. B. sodium or potassium carbonate, and also a copper salt such as copper (I) acetate or copper (I) bromide to be added.
<I> Example: </I> 12 parts of 1.-amino-6-fluoroanthraquinone and 7.4 parts of 4'-chloro-1,1'-diphenyl-4-carboxylic acid chloride are stirred for 2 hours at 125 to 130 When it cools, the dye which has precipitated out in yellow needles is filtered off with suction, washed with nitrobenzene and boiling alcohol and dried.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH289992T | 1951-07-10 | ||
CH294951T | 1951-07-10 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH294951A true CH294951A (en) | 1953-11-30 |
Family
ID=25732923
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH294951D CH294951A (en) | 1951-07-10 | 1951-07-10 | Process for the production of a vat dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH294951A (en) |
-
1951
- 1951-07-10 CH CH294951D patent/CH294951A/en unknown
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