CH148979A - Process for the preparation of an azo dye. - Google Patents
Process for the preparation of an azo dye.Info
- Publication number
- CH148979A CH148979A CH148979DA CH148979A CH 148979 A CH148979 A CH 148979A CH 148979D A CH148979D A CH 148979DA CH 148979 A CH148979 A CH 148979A
- Authority
- CH
- Switzerland
- Prior art keywords
- preparation
- azo dye
- fastness
- dye
- produced
- Prior art date
Links
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Darstellung eines Azofarbstoffes. Gegenstand der vorliegenden Erfindung ist ein Verfahren zur Darstellung eines Azo- farbstoffes, welches dadurch gekennzeichnet ist, dass man die Diazoverbindung von 5-Chlor- 2-aminobenzoesäuremethylester mit 2 . 3-Oxy- naphtoesäure-alpb.a-naphtylamid kuppelt. Die Einwirkung der beiden Komponenten aufein ander kann auch in Gegenwart eines Sub strates erfolgen.
Der in- Substanz hergestellte Farbstoff bildet ein rotes Pulver und liefert, wenn auf der Faser erzeugt, ein lebhaftes Rot von sehr guter Lichtechtheit, Waschechtheit und guter Laugenkochechtheit.
<I>Beispiel:</I> 18,5 Gewichtsteile 5-Chlor-2-aminobenzoe- säuremethylester werden in bekannter Weise mit Salzsäure und Natriumnitrit diazotiert. Die nötigenfalls filtrierte Diazolösung wird bei 0 bis 5 C rnit einer ätzalkalischen wässerigen Lösung von 31,3 Gewichtsteilen 2 . 3-Oxynaphtoesäure-alpha-naphtylamid ver einigt. Der Farbstoff fällt sofort in Form roter Flocken aus. Nach dem Filtrieren wird mit Wasser gewaschen und getrocknet.
Die Darstellung des Farbstoffes kann auch in Gegenwart eines Substrates erfolgen. Wird der Farbstoff auf der Faser erzeugt, so erhält man ein lebhaftes Rot von sehr guter Licht echtheit; Waschechtheit und guter Laugen kochechtheit.
Process for the preparation of an azo dye. The present invention relates to a process for the preparation of an azo dye, which is characterized in that the diazo compound of 5-chloro-2-aminobenzoic acid methyl ester with 2. 3-oxynaphthoic acid alpb.a-naphthylamide couples. The action of the two components on one another can also take place in the presence of a substrate.
The dyestuff produced in substance forms a red powder and, when produced on the fiber, provides a vivid red with very good fastness to light, fastness to washing and good fastness to lye boiling.
<I> Example: </I> 18.5 parts by weight of 5-chloro-2-aminobenzoic acid methyl ester are diazotized in a known manner with hydrochloric acid and sodium nitrite. The diazo solution, filtered if necessary, is mixed at 0 to 5 C with a caustic alkaline aqueous solution of 31.3 parts by weight of 2. 3-oxynaphthoic acid-alpha-naphthylamide united. The dye immediately precipitates in the form of red flakes. After filtering, it is washed with water and dried.
The preparation of the dye can also take place in the presence of a substrate. If the dye is produced on the fiber, a vivid red with very good light fastness is obtained; Washfastness and good lye fastness to boil.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE148979X | 1928-09-18 | ||
CH145153T | 1929-09-13 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH148979A true CH148979A (en) | 1931-08-15 |
Family
ID=25714617
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH148979D CH148979A (en) | 1928-09-18 | 1929-09-13 | Process for the preparation of an azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH148979A (en) |
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1929
- 1929-09-13 CH CH148979D patent/CH148979A/en unknown
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