CH151170A - Process for the preparation of a wool dye. - Google Patents
Process for the preparation of a wool dye.Info
- Publication number
- CH151170A CH151170A CH151170DA CH151170A CH 151170 A CH151170 A CH 151170A CH 151170D A CH151170D A CH 151170DA CH 151170 A CH151170 A CH 151170A
- Authority
- CH
- Switzerland
- Prior art keywords
- preparation
- wool
- parts
- dye
- wool dye
- Prior art date
Links
Landscapes
- Coloring (AREA)
Description
Terfahren zur Darstellung eines Wollfarbstoffes. Wie gefunden wurde, gelangt man zu einem neuen wert-vollen Farbstoff, der Wolle in rotbraunen, gut egalisierenden Tönen von sehr guter LichtecUtheit färbt, wenn man <B>1 Hol.</B> 2'-Chlor-2, 6-diaminodiphenylamin-4- sulfosäure mit<B>1</B> Mol. 2. 4. 6-Trinitroalkoxy- benzol kondensiert. Hierbei findet zunächst.
die zu erwartende Reaktion zwischen der Alkoxygruppe und einer Aminogruppe statt, bei weiterem Erhitzen in Gegenwart von Alkali tritt dann unter Abspaltung von Alka-Iinitrit eine innere Kondensation ein.
<I>Beispiel:</I> <B>31,335</B> Teile 2-Chlor-2. 6-diaminodiplie- nylamin-4-sulfosäure, erhalten durch Kon densation von 2. 6-Dinitrochlorbenzal-#l-sulio- #äure mit 2-Chloranilin und folgende Reduk tion der Nitrogruppen, werden in<B>500</B> Teilen Wasser neutral gelöst und bei<B>70</B> bis<B>80 '</B> mit 24 Teilen 2. 4.
6-Trinitraanisol, welches man allmählich unter Rühren zugibt, kon- densiert. Gleichzeitig lässt man eine Lösun,(., von <B>6</B> Teilen Natriumkarbonat in<B>60</B> Teilen g"asser zutropfen. Nachdem alles Trinitr.)- anisol umgesetzt ist, gibt man noch<B>6</B> Teile Natriumkarbonat hinzu und erhitzt einr,
Stunde auf<B>90</B> '. Der Farbstoff wird durel- Aussalzen abgeschieden und getrocknet. Er bildet ein schwarzes Pulver.
Terfahren for the representation of a wool dye. It has been found that a new valuable dye is obtained which dyes wool in reddish-brown, well-leveling shades of very good lightness if <B> 1 Hol. </B> 2'-chloro-2,6-diaminodiphenylamine is used -4- sulfonic acid with <B> 1 </B> Mol. 2. 4. 6-trinitroalkoxybenzene condensed. This takes place first.
the expected reaction between the alkoxy group and an amino group takes place; on further heating in the presence of alkali an internal condensation occurs with elimination of alkali initrite.
<I> Example: </I> <B> 31,335 </B> parts 2-chloro-2. 6-diaminodiplanylamine-4-sulfonic acid, obtained by condensation of 2. 6-dinitrochlorobenzal- # l-sulio- # acid with 2-chloroaniline and the subsequent reduction of the nitro groups, are in 500 parts Water dissolved neutrally and at <B> 70 </B> to <B> 80 '</B> with 24 parts 2. 4.
6-trinitraanisole, which is added gradually with stirring, condenses. At the same time, a solution (., Of <B> 6 </B> parts of sodium carbonate in <B> 60 </B> parts of g "ater. After all of the trinitrate.) - anisole has been converted, <B > 6 </B> parts of sodium carbonate and heat in the oven,
Hour to <B> 90 </B> '. The dye is deposited by salting out and dried. It forms a black powder.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE151170X | 1929-08-17 | ||
CH147460T | 1931-06-15 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH151170A true CH151170A (en) | 1931-11-30 |
Family
ID=25715038
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH151170D CH151170A (en) | 1929-08-17 | 1930-03-12 | Process for the preparation of a wool dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH151170A (en) |
-
1930
- 1930-03-12 CH CH151170D patent/CH151170A/en unknown
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