CH301816A - Process for the preparation of a monoazo dye. - Google Patents
Process for the preparation of a monoazo dye.Info
- Publication number
- CH301816A CH301816A CH301816DA CH301816A CH 301816 A CH301816 A CH 301816A CH 301816D A CH301816D A CH 301816DA CH 301816 A CH301816 A CH 301816A
- Authority
- CH
- Switzerland
- Prior art keywords
- dye
- tones
- monoazo dye
- bath
- preparation
- Prior art date
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
- C09B45/00—Complex metal compounds of azo dyes
- C09B45/02—Preparation from dyes containing in o-position a hydroxy group and in o'-position hydroxy, alkoxy, carboxyl, amino or keto groups
- C09B45/14—Monoazo compounds
- C09B45/16—Monoazo compounds containing chromium
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
Verfahren zur Herstellung eines Monoazofarbstoffes. Es wurde gefunden, dass man zu einem neuen, wertvollen Monoazofarbstoff gelangt, wenn man 1-Phenylamino-S-oxynaphthalin-4- sulfonsäure mit diazotiertein 6--,\Titro-2-aniino- 1-oxybenzol-4-m,ethylsulfon vereinigt.
Der neue Farbstoff bildet ein dunkles Pul ver, das sieh in Wasser mit blauer, in kon zentrierter Schwefelsäure mit bordeauxroter Farbe löst und Wolle aus essigsaurem Bade in blauen Tönen färbt, die durch Nachehro- inieren in ein sehr echtes Grün übergehen.. Der Farbstoff eignet sich auch vorzüglich zum Färben nach dem Einbadchromierverfahren, wobei ebenfalls echte grüne Töne erhalten werden, Die Dianotierung des 6-Nitro-2-amino-l- oxybenzol-4-methylsitlfons kann nach an. sich bekannten Methoden erfolgen, zum Beispiel mittels Natriumnitrit und Salzsäure.
Die Kupplung wird beim vorliegenden Verfahren mit Vorteil in alkalischem Medium durchgeführt.
<I>Beispiel:</I> 23,2 Teile 6-Nitro-2-amina-l-oxybenzol-4- metliylsulfon werden in üblicher Weise in salz saurer Lösung mit Natriumnitrit dianotiert. Die mit Natriumcarbonat neutralisierte Di- azoverbindung vereinigt man mit einer mit Eis abgekühlten Lösung, hergestellt aus 33 Teilen 1-Phenylamino-S-oxynaphthalin-4- sulfonsä.ure, 50 Volumteilen Wasser,
50 Vo- lumteilen 2n - Natriumhy droxydlösung und 50 Volumteilen einer 15prozentigen Natrium carbonatlösung. Nach beendeter Kupplung wird der abgeschiedene Farbstoff abfiltriert, mit verdünnter Natriumchloridlösung gewa- sehen und getrocknet.
Process for the preparation of a monoazo dye. It has been found that a new, valuable monoazo dye is obtained if 1-phenylamino-S-oxynaphthalene-4-sulfonic acid is combined with diazotized 6 -, \ titro-2-aniino-1-oxybenzene-4-m, ethyl sulfone .
The new dye forms a dark powder that dissolves in water with a blue color, in concentrated sulfuric acid it dissolves with a burgundy red color, and dyes wool from an acetic acid bath in blue tones, which turn into a very real green through subsequent ironing. The dye is suitable is also excellent for dyeing by the single-bath chromium plating process, which also gives real green tones. The dianotation of 6-nitro-2-amino-l-oxybenzene-4-methylsitlfons can also known methods are carried out, for example using sodium nitrite and hydrochloric acid.
In the present process, the coupling is advantageously carried out in an alkaline medium.
<I> Example: </I> 23.2 parts of 6-nitro-2-amina-1-oxybenzene-4-methylsulfone are dianotized with sodium nitrite in the usual way in a salt-acidic solution. The diazo compound neutralized with sodium carbonate is combined with a solution cooled with ice, prepared from 33 parts of 1-phenylamino-S-oxynaphthalene-4-sulfonic acid, 50 parts by volume of water,
50 parts by volume of 2N sodium hydroxide solution and 50 parts by volume of a 15 percent sodium carbonate solution. After the coupling has ended, the deposited dye is filtered off, washed with dilute sodium chloride solution and dried.
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH301816T | 1952-03-19 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH301816A true CH301816A (en) | 1954-09-30 |
Family
ID=4491173
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH301816D CH301816A (en) | 1952-03-19 | 1952-03-19 | Process for the preparation of a monoazo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH301816A (en) |
-
1952
- 1952-03-19 CH CH301816D patent/CH301816A/en unknown
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