CH166665A - Process for the preparation of an o-oxyazo dye. - Google Patents
Process for the preparation of an o-oxyazo dye.Info
- Publication number
- CH166665A CH166665A CH166665DA CH166665A CH 166665 A CH166665 A CH 166665A CH 166665D A CH166665D A CH 166665DA CH 166665 A CH166665 A CH 166665A
- Authority
- CH
- Switzerland
- Prior art keywords
- dye
- preparation
- dioxyquinoline
- oxyazo
- benzo
- Prior art date
Links
Landscapes
- Coloring (AREA)
Description
Verfahren zur Herstellung eines o-Ogyazofarbstoffes. Nach dem durch das Hauptpatent ge schützten Verfahren erhält man einen Wolle in Gegenwart von Chrombeizen echt anfär benden Farbstoff, wenn man 4-Chlor-2-diazo- 1-oxybenzol-6-sulfosäure mit 7.8-Benzo-2.4- dioxychinolin kuppelt.
Wie nun weiter gefunden wurde, erhält man einen Farbstoff mit ähnlichen guten Eigenschaften, wenn man an Stelle des 7.8- Benzo-2.4-dioxychinolins 5.6-Benzo-2.4- dioxychinolin, als Azokomponente wählt.
Man erhält dieses letztgenannte Dioxy- chinolin ganz ähnlich, wie das 7.8-Benzo- 2.4-dioxychinolin, nämlich durch Erhitzen von 2-Naphthylamin und Malonester.
<I>Beispiel:</I> 22,4 Teile 4-Chlor-2-amino-l-oxybenzol-6- sulfosäure werden mit etwa 300 Teilen Was ser angeschlämmt und nach Zusatz von 5 Teilen Salzsäure von 121 B6 mit 6,9 Teilen Natriumnitrit bei<B>100</B> diazotiert. Die fertige Diazoverbindung läuft in eine kalte Lösung von 23 Teilen 5.6-Benzo-2.4-dioxychinolin und 6 Teilen Natriumhydroxyd in etwa 500 Teilen Wasser. Nach beendeter .Kombination wird der Farbstoff in bekannter Weise auf gearbeitet.
Er stellt in trockenem Zustand ein dunkles Pulver dar und färbt Wolle nach dem Einbad-Chromverfahren in violetten Tönen von sehr guter Wasch- und Walkecht- heit an.
Process for the preparation of an o-ogyazo dye. According to the process protected by the main patent ge one obtains a wool in the presence of chrome stains really staining dye if 4-chloro-2-diazo-1-oxybenzene-6-sulfonic acid is coupled with 7.8-benzo-2.4-dioxyquinoline.
As has now been found, a dye with similar good properties is obtained if 5.6-benzo-2.4-dioxyquinoline is chosen as the azo component instead of 7.8-benzo-2.4-dioxyquinoline.
This last-mentioned dioxyquinoline is obtained in a very similar way to 7.8-benzo-2,4-dioxyquinoline, namely by heating 2-naphthylamine and malonic ester.
<I> Example: </I> 22.4 parts of 4-chloro-2-amino-1-oxybenzene-6-sulfonic acid are slurried with about 300 parts of water and, after addition of 5 parts of hydrochloric acid, 121 B6 with 6.9 Share sodium nitrite at <B> 100 </B> diazotized. The finished diazo compound runs into a cold solution of 23 parts of 5.6-benzo-2.4-dioxyquinoline and 6 parts of sodium hydroxide in about 500 parts of water. After the combination has ended, the dye is worked up in a known manner.
When dry, it is a dark powder and uses the single-bath chrome process to dye wool in purple tones that are very washable and milled.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE166665X | 1932-04-18 | ||
CH164201T | 1932-11-11 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH166665A true CH166665A (en) | 1934-01-15 |
Family
ID=25717941
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH166665D CH166665A (en) | 1932-04-18 | 1932-11-11 | Process for the preparation of an o-oxyazo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH166665A (en) |
-
1932
- 1932-11-11 CH CH166665D patent/CH166665A/en unknown
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