CH199970A - Process for the preparation of an azo dye. - Google Patents
Process for the preparation of an azo dye.Info
- Publication number
- CH199970A CH199970A CH199970DA CH199970A CH 199970 A CH199970 A CH 199970A CH 199970D A CH199970D A CH 199970DA CH 199970 A CH199970 A CH 199970A
- Authority
- CH
- Switzerland
- Prior art keywords
- dye
- nitro
- amino
- leather
- coupled
- Prior art date
Links
Description
Verfahren zur Herstellung eines Azofarbstoffes. Nach dem im Hauptpatent beschriebenen Verfahren erhält man einen Leder in klar rotbraunen Tönen von vorzüglicher Echtheit anfärbenden Farbstoff, wenn man diazo- tierte 1-Amino-8-ogynaphthalin-3.6-disulfo- säure mit 1.
3-Diogybenzol kuppelt, den so erhaltenen Monoazofarbstoff mit diazotier- tem 4-Nitro-2-amino-l-ogybenzol behandelt und schliesslich den dann erhaltenen, Disazo- farbstoff in alkalischem Medium in die Kupferverhindung überführt.
Wie nun weitergefunden wurde, erhält man einen Farbstoff von ähnlichen Eigen schaften, wenn man den nach dem Haupt patent erhältlichen Disazofarbstoff mit di- azotierter 4'-Nitro-4-aminodiphenylamin-2'- sulfosäure weiter behandelt und dann in die Kupferverbindung überführt.
<I>Beispiel:</I> 34,1 Teile 1-Amino-8-ogynaphthalin-,3i. 6- @disulfosäure (saures Na-Salz) werden in be- kannter Weise diazotiert und mit einer alka lisch gehaltenen Lösung von 11 Teilen 1. 3- Diogybenzol vereinigt.
Zu dem Monoazofarb- stoff lässt man ebenfalls. in alkalisch gehal tenem Medium: eine aus 15,4 Teilen 4-Nitro- 2-amino-l-ogybenzol bereitete Diazoverbin- dung hinzulaufen. Dann bereitet man aus 30,9 Teilen 4'-Nitro-4-aminodiphenylamin-2'- sulfosäure die Diazoverbindung und gibt sie in, die alkalisch gehaltene Lösung des vor gängig erhaltenen Farbstoffes.
Nach beende ter Kupplung wird der so erhaltene Farb stoff in alkalischem Medium mit 50 Teilen Kupfersulfat erwärmt. Er färbt Chromleder und vegetabilisch gegerbtes Leder in braunen Tönen von guter Echtheit.
Process for the preparation of an azo dye. According to the process described in the main patent, a leather in clear red-brown shades of excellent fastness-dyeing dye is obtained if diazotized 1-amino-8-ogynaphthalene-3,6-disulfonic acid is mixed with 1.
3-Diogybenzene is coupled, the monoazo dye thus obtained is treated with diazotized 4-nitro-2-amino-1-ogybenzene and finally the disazo dye obtained is converted into the copper compound in an alkaline medium.
As has now been found, a dye with similar properties is obtained if the disazo dye obtainable according to the main patent is treated further with diazotized 4'-nitro-4-aminodiphenylamine-2'-sulfonic acid and then converted into the copper compound.
<I> Example: </I> 34.1 parts of 1-amino-8-ogynaphthalene-, 3i. 6- @ disulfonic acid (acidic sodium salt) are diazotized in a known manner and combined with an alkaline solution of 11 parts of 1,3-diogybenzene.
The monoazo dye is also allowed. in an alkaline medium: a diazo compound prepared from 15.4 parts of 4-nitro-2-amino-1-ogybenzene is added. The diazo compound is then prepared from 30.9 parts of 4'-nitro-4-aminodiphenylamine-2'-sulfonic acid and is added to the alkaline solution of the dye previously obtained.
After the coupling has ended, the dye thus obtained is heated in an alkaline medium with 50 parts of copper sulfate. It dyes chrome leather and vegetable tanned leather in brown shades of good fastness.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE199970X | 1936-07-02 | ||
CH198141T | 1937-05-08 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH199970A true CH199970A (en) | 1938-09-15 |
Family
ID=25723080
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH199970D CH199970A (en) | 1936-07-02 | 1937-05-08 | Process for the preparation of an azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH199970A (en) |
-
1937
- 1937-05-08 CH CH199970D patent/CH199970A/en unknown
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