CH186739A - Process for the preparation of an azo dye. - Google Patents
Process for the preparation of an azo dye.Info
- Publication number
- CH186739A CH186739A CH186739DA CH186739A CH 186739 A CH186739 A CH 186739A CH 186739D A CH186739D A CH 186739DA CH 186739 A CH186739 A CH 186739A
- Authority
- CH
- Switzerland
- Prior art keywords
- azo dye
- preparation
- dye
- amino
- acid
- Prior art date
Links
Landscapes
- Coloring (AREA)
Description
Verfahren zur Herstellung eines Azofarbstof%s. Es wurde gefunden, dass man wertvolle Azofarbstoffe erhält, wenn man die Diazo- verbindungen von Aminen der allgemeinen Formel
EMI0001.0005
worin X einen Substituenten, insbesondere einen nichtsaurere Substituenten, wie Alkyl, Aryl, Aralkyl, Alkoxy, Aralkoxy oder Aryl- oxy bedeutet und R für Alkyl, Aryl,
Ar- alkyl, Alkoxy, Aralkoxy ,Aryloxy oder die Aminogruppe steht, deren Wasserstoffatome ganz oder teilweise durch gleiche oder ver schiedene Alkyl-, Aryl- oder Aralkylreste substituiert sein können, mit 2-Aminonaph- thalinsulfonsäuren oder ihren Substitutions- produkten in saurem Medium vereinigt.
Die so erhältlichen Farbstoffe haben ein gutes Egalisierungsvermögen und färben Wolle im allgemeinen in blauen Tönen von guter Walkechtheit. Die Färbungen können sich ausserdem durch eine gute Abendfarbe auszeichnen.
Gegenstand des vorliegenden Patentes ist ein Verfahren zur Herstellung eines Azo- farbstoffes. Es ist dadurch gekennzeichnet. dass man das diazotierte 5-Nitro-2-amino-l- methoxybenzol-3-suHäthylanilid mit 2 Me- thylamino - 8 - oxynaphthalin - 6 - sulfosäure in saurem Medium kuppelt.
<I>Beispiel:</I> 351 Gewichtsteile 5-Nitro-2-amino-l-me- thoxybenzol-3-sulfäthylanilid werden mit 69 Gewichtsteilen Natriumnitrit und Salzsäure diazotiert und essigsauer mit 253 Gewichts teilen 2-Methylamino-8-oxynaphthalin-6-sul- fosäure gekuppelt. Der isolierte Farbstoff färbt Wolle aus saurem Bade in klaren, sehr grünsticlhig blauen Tönen von ausgezeichne ter Abendfarbe.
Process for the preparation of an azo dye% s. It has been found that valuable azo dyes are obtained if the diazo compounds of amines of the general formula are used
EMI0001.0005
wherein X is a substituent, in particular a non-acidic substituent, such as alkyl, aryl, aralkyl, alkoxy, aralkoxy or aryloxy and R is alkyl, aryl
Aralkyl, alkoxy, aralkoxy, aryloxy or the amino group, the hydrogen atoms of which can be completely or partially substituted by identical or different alkyl, aryl or aralkyl radicals, combined with 2-aminonaphthalene sulfonic acids or their substitution products in an acidic medium .
The dyes obtainable in this way have good leveling properties and generally dye wool in blue shades of good millfastness. The colors can also be characterized by a good evening color.
The present patent relates to a process for the production of an azo dye. It is characterized by it. that the diazotized 5-nitro-2-amino-1-methoxybenzene-3-suHäthylanilid with 2 methylamino-8-oxynaphthalene-6-sulfonic acid is coupled in an acidic medium.
<I> Example: </I> 351 parts by weight of 5-nitro-2-amino-1-methoxybenzene-3-sulfethylanilide are diazotized with 69 parts by weight of sodium nitrite and hydrochloric acid and acetic acid with 253 parts by weight of 2-methylamino-8-oxynaphthalene 6-sulphonic acid coupled. The isolated dye dyes wool from an acid bath in clear, very greenish blue tones of an excellent evening color.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE186739X | 1934-02-24 | ||
CH182049T | 1935-01-31 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH186739A true CH186739A (en) | 1936-09-30 |
Family
ID=25720652
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH186739D CH186739A (en) | 1934-02-24 | 1935-01-31 | Process for the preparation of an azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH186739A (en) |
-
1935
- 1935-01-31 CH CH186739D patent/CH186739A/en unknown
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CH186739A (en) | Process for the preparation of an azo dye. | |
CH186740A (en) | Process for the preparation of an azo dye. | |
CH182049A (en) | Process for the preparation of an azo dye. | |
CH186741A (en) | Process for the preparation of an azo dye. | |
DE676785C (en) | Process for the production of azo dyes | |
AT149986B (en) | Process for the preparation of water-insoluble monoazo dyes. | |
AT155466B (en) | Process for the production of water-insoluble azo dyes. | |
DE409281C (en) | Process for the production of acidic monoazo dyes for wool | |
DE641569C (en) | Process for the preparation of monoazo dyes | |
AT117043B (en) | Process for the preparation of monoazo dyes. | |
DE682540C (en) | Process for the preparation of monoazo dyes | |
AT148468B (en) | Process for the preparation of monoazo dyes. | |
AT106016B (en) | Process for the preparation of monoazo dyes. | |
AT141136B (en) | Process for the preparation of water-insoluble monoazo dyes. | |
DE695402C (en) | Process for the preparation of disazo dyes | |
AT88347B (en) | Process for the preparation of monoazo dyes. | |
CH190034A (en) | Process for the preparation of an azo dye. | |
CH311073A (en) | Process for the preparation of a water-insoluble disazo dye. | |
CH199092A (en) | Process for the preparation of an azo dye. | |
CH182266A (en) | Process for the preparation of a new disazo dye. | |
CH187431A (en) | Process for the production of an acidic wool dye of the anthraquinone series. | |
CH169701A (en) | Process for the preparation of a monoazo dye. | |
CH185674A (en) | Process for the preparation of a monoazo dye. | |
CH183592A (en) | Process for the preparation of an azo dye. | |
CH235458A (en) | Process for the preparation of a water-soluble monoazo dye. |