CH170917A - Process for the preparation of an azo dye. - Google Patents
Process for the preparation of an azo dye.Info
- Publication number
- CH170917A CH170917A CH170917DA CH170917A CH 170917 A CH170917 A CH 170917A CH 170917D A CH170917D A CH 170917DA CH 170917 A CH170917 A CH 170917A
- Authority
- CH
- Switzerland
- Prior art keywords
- preparation
- aminobenzene
- azo dye
- dye
- parts
- Prior art date
Links
Landscapes
- Coloring (AREA)
Description
Verfahren zur 1)arstellunb eines Azofarbstofes. Nach dem im Hauptpatent beschriebenen Verfahren erhält man einen blauen Acetat seidenfarbstoff, wenn man diazotiertes G Brom - 2 . 4 - dinitro - 1- aminobenzol mit 1- Aminonaphthalin kuppelt.
Wie nun weiter gefunden wurde, er hält man einen Farbstoff mit ganz ähnlichen Eigenschaften, wenn man 6 - Chlor - 2. 4 - di- nitro - 1 - aminobenzol diazotiert ufd mit Di - (oxyäthyl) - aminobenzol kuppelt.
<I>Beispiel:</I> Man bereitet eine Diazolösung, indem man bei 50 bis 60 22 Teile 6; - Chlor - 2. 4 dinitro - 1 - aminobenzol in durch Eintragen von 6,9 Teilen Natriumnitrit in 120 Teile konz. Schwefelsäure bereitete Nitrosyl- schwefelsäure einrührt und die Masse hier auf durch Aufgiessen auf Eis stark verdünnt.
Die filtrierte schwefelsaure Diazolösung läuft in eine kalte Lösung von 18,1 Teilen Di- (oxyäthyl)- - aminobenzol in 500 Teilen Was ser und 11 Teilen Salzsäure<B>23'</B> B6 ein. Han stumpft mit so viel Natriumacetat ab, dass die Kupplung im Verlauf von einigen Stunden beendet ist. Der Farbstoff wird wie üblich aufgearbeitet. Er färbt Acetatseide lichtecht blaurot an.
Method for 1) preparation of an azo dye. According to the process described in the main patent, a blue acetate silk dye is obtained if diazotized G bromine - 2. 4 - dinitro - 1 - aminobenzene couples with 1 - aminonaphthalene.
As has now been further found, a dye with very similar properties is obtained if 6 - chloro - 2, 4 - nitro - 1 - aminobenzene is diazotized and coupled with di - (oxyethyl) - aminobenzene.
<I> Example: </I> A diazo solution is prepared by adding 22 parts 6; to 50 to 60; - Chlorine - 2.4 dinitro - 1 - aminobenzene in by adding 6.9 parts of sodium nitrite in 120 parts of conc. Sulfuric acid, stir in nitrosylsulphuric acid and dilute the mass here by pouring it onto ice.
The filtered sulfuric acid diazo solution runs into a cold solution of 18.1 parts of di- (oxyethyl) - aminobenzene in 500 parts of water and 11 parts of hydrochloric acid 23 'B6. Han dulls with so much sodium acetate that the coupling is complete within a few hours. The dye is worked up as usual. It stains acetate silk lightfast blue-red.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE170917X | 1932-07-08 | ||
CH168144T | 1933-04-27 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH170917A true CH170917A (en) | 1934-07-31 |
Family
ID=25718517
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH170917D CH170917A (en) | 1932-07-08 | 1933-04-27 | Process for the preparation of an azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH170917A (en) |
-
1933
- 1933-04-27 CH CH170917D patent/CH170917A/en unknown
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