DE163141C - - Google Patents
Info
- Publication number
- DE163141C DE163141C DE1904163141D DE163141DA DE163141C DE 163141 C DE163141 C DE 163141C DE 1904163141 D DE1904163141 D DE 1904163141D DE 163141D A DE163141D A DE 163141DA DE 163141 C DE163141 C DE 163141C
- Authority
- DE
- Germany
- Prior art keywords
- methyl
- ketol
- molecule
- methylindole
- parts
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B35/00—Disazo and polyazo dyes of the type A<-D->B prepared by diazotising and coupling
- C09B35/02—Disazo dyes
- C09B35/039—Disazo dyes characterised by the tetrazo component
- C09B35/08—Disazo dyes characterised by the tetrazo component the tetrazo component being a derivative of biphenyl
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
PATENTAMT,PATENT OFFICE,
KLASSE 22 a. CLASS 22 a.
Im Hauptpatent 160674 wurde ein Verfahren zur Darstellung von walkechten Disazofarbstoffen beschrieben, welches darin besteht, daß man die Tetrazoverbindungen der Benzidin- oder Tolidin-m-disulfosäure mit 2 Molekülen Methylketol (a-Methylindol) oder in beliebiger Reihenfolge mit 1 Molekül Methylketol (a-Methylindol) und 1 Molekül i-Phenyl-3-methyl-5-pyrazolon kuppelt.In the main patent 160674, a process for the preparation of walk-fast disazo dyes was found described, which consists in the fact that the tetrazo compounds of benzidine or tolidine-m-disulfonic acid with 2 molecules of methyl ketol (a-methylindole) or in any order with 1 molecule Methyl ketol (a-methylindole) and 1 molecule of i-phenyl-3-methyl-5-pyrazolone couples.
Es wurde nun gefunden, daß, wenn man die genannten Tetrazoverbindungen der Benzidin- bezw. Tolidinsulfosäuren der Formeln :It has now been found that if you use the tetrazo compounds mentioned of the benzidine respectively Tolidinsulfonic acids of the formulas:
JVÄ,-JVÄ, -
bezw.respectively
NH9-'NH 9 - '
>-NH> -NH
SO3HSO 3 H
>-NH,> -NH,
SO3HSO 3 H
SO3HSO 3 H
CHCH
in beliebiger Reihenfolge mit ι Molekül Methylketol (a-Methylindol) und ι Molekül ß-Naphtol kuppelt, man zu orangefarbenen Wollfarbstoffen gelangt, die sich ebenfalls durch die technisch äußerst wichtige Eigenschaft auszeichnen, daß sie bereits in direkter Färbung gegen weiße Wolle und gegen weiße Baumwolle walkecht sind.in any order with ι molecule methyl ketol (a-methylindole) and ι molecule ß-Naphtol couples, one arrives at orange-colored wool dyes, which are also distinguished by the technically extremely important property that they are already in direct Dyeing against white wool and against white cotton are non-squeeze.
Beispiel.
37,2 Teile Tolidindisulfosäure werdenExample.
37.2 parts of tolidinedisulfonic acid are used
3535
inin
bekannter Weise durch Zusatz von Salzsäure und 13,8 Teilen Natriumnitrit diazotiert, zu der so erhaltenen Tetrazoverbindung 14 Teile Methylketol, gelöst in 100 Teilen Salzsäure (20° Be.), zugegeben, ein Überschuß von essigsaurem Natrium zugesetzt und gerührt, bis daß die Bildung des Zwischenproduktes beendet ist. Man läßt darauf eine Lösung von 14,4 Teilen ß-Naphtol in verdünnter Natronlauge zulaufen und macht durch Zusatz von Sodalösung alkalisch. Nach einigen Stunden ist die Kuppelung beendet. Es wird nun der neue Farbstoff isoliert. Er färbt Wolle in klaren, orangen Tönen an.known manner by adding hydrochloric acid and 13.8 parts of sodium nitrite diazotized to of the tetrazo compound thus obtained, 14 parts of methyl ketol, dissolved in 100 parts of hydrochloric acid (20 ° Be.), Added, added an excess of sodium acetate and stirred, until the formation of the intermediate product has ended. A solution is left on it run in from 14.4 parts of ß-naphthol in dilute sodium hydroxide solution and make it by adding of soda solution alkaline. The coupling is finished after a few hours. It will now the new dye is isolated. He dyes wool in clear, orange tones.
Der analoge Farbstoff aus der Benzidindisulfosäure färbt ebenfalls Wolle orange.The analogous dye from benzidine disulfonic acid also dyes wool orange.
Claims (1)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AT23906D AT23906B (en) | 1904-10-31 | 1905-07-22 | Process for the preparation of orange disazo dyes for wool. |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE160674T |
Publications (1)
Publication Number | Publication Date |
---|---|
DE163141C true DE163141C (en) |
Family
ID=5681354
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE1904160674D Expired - Lifetime DE160674C (en) | 1904-05-09 | 1904-05-09 | |
DE1904163141D Expired - Lifetime DE163141C (en) | 1904-10-31 | 1904-10-31 |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE1904160674D Expired - Lifetime DE160674C (en) | 1904-05-09 | 1904-05-09 |
Country Status (1)
Country | Link |
---|---|
DE (2) | DE160674C (en) |
-
1904
- 1904-05-09 DE DE1904160674D patent/DE160674C/de not_active Expired - Lifetime
- 1904-10-31 DE DE1904163141D patent/DE163141C/de not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
DE160674C (en) |
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