CH267611A - Process for the preparation of an oxyacylaminoazo dye. - Google Patents
Process for the preparation of an oxyacylaminoazo dye.Info
- Publication number
- CH267611A CH267611A CH267611DA CH267611A CH 267611 A CH267611 A CH 267611A CH 267611D A CH267611D A CH 267611DA CH 267611 A CH267611 A CH 267611A
- Authority
- CH
- Switzerland
- Prior art keywords
- dye
- acid
- preparation
- oxyacetylaminoazo
- new
- 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
- C09B43/00—Preparation of azo dyes from other azo compounds
- C09B43/12—Preparation of azo dyes from other azo compounds by acylation of amino groups
- C09B43/124—Preparation of azo dyes from other azo compounds by acylation of amino groups with monocarboxylic acids, carbamic esters or halides, mono- isocyanates, or haloformic acid esters
- C09B43/128—Aliphatic, cycloaliphatic or araliphatic acids
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
- Paper (AREA)
Description
<B>Zusatzpatent</B> zum Hauptpatent Nr. 262278. Verfahren zur Herstellung eines Oxyacylaminoazofarbstoffes. Das vorliegende Patent betrifft ein Ver fahren zur Herstellung eines neuen, Oxyacetyl- aminoazofarbstoffes und ist dadurch gekenn zeichnet, dass man den Monoazofarbstoff, den man durch Vereinigen von diazot.ierter Anilin-2,5-disulfonsäure mit 2-Amino-8-oxy- naphthalin-6-sulfonsäure in saurem Medium erhält,
mit Acety lierungsmitteln behandelt und hierauf den bei dieser Behandlung mit entstandenen Anteil. an N.0-Acety lprodukt durch Einwirkung von Verseifungsmitteln in den 0xyaeetylaminoazofarbstoff überführt.
Im Beispiel bedeuten Teile Gewichtsteile. <I>Beispiel:</I> 47 Teile des Monoazofa.rbstoffes, den man durch Vereinigen von diazotiertcr Anilin-2,5- disulfonsäure mit 2-Amino-8-oxynaphthalin-6- sulfonsäure in saurem Medium erhält, wer den in das Gemisch von 50 Teilen Mono hydrat und 150 Teilen Essigsäureanhydrid bei Zimmertemperatur eingetragen und wäh rend mehrerer Stunden gerührt. Die Kon densation ist, beendigt, sobald keine freie Aminogruppe mehr nachgewiesen werden kann.
Hierauf verdünnt man mit Aceton, wo bei das gelbe Acetylierungsprodukt in gut filtrierbarer Form ausfällt. Man filtriert ab, wäscht mit Aceton nach und erwärmt den Rückstand zwecks Abspaltung des in die Hydroxylgruppe eingetretenen Acetylrestes während kurzer Zeit in 5prozentiger Soda lösung auf 40 bis 50 . Hierauf salzt man aus, filtriert und trocknet. Der entstandene Farbstoff, ein braunes Pulver, färbt Wolle aus saurem Bade in orangeroten Tönen und kuppelt glatt mit Diazoverbindungen. Er löst sich in konzentrierter Schwefelsäure mit blauer, der Ausgangsfarbstoff dagegen mit orangeroter Farbe.
<B> Additional patent </B> to main patent no. 262278. Process for the preparation of an oxyacylaminoazo dye. The present patent relates to a process for the preparation of a new, oxyacetyl aminoazo dye and is characterized in that the monoazo dye, which is obtained by combining diazotized aniline-2,5-disulfonic acid with 2-amino-8-oxy- receives naphthalene-6-sulfonic acid in an acidic medium,
Treated with acetylating agents and then the portion resulting from this treatment. on N.0 acetyl product converted into the 0xyaeetylaminoazo dye by the action of saponifying agents.
In the example, parts mean parts by weight. <I> Example: </I> 47 parts of the monoazofa dye, which is obtained by combining diazotized aniline-2,5-disulfonic acid with 2-amino-8-oxynaphthalene-6-sulfonic acid in an acidic medium Mixture of 50 parts of monohydrate and 150 parts of acetic anhydride entered at room temperature and stirred during several hours rend. The condensation is ended as soon as no more free amino groups can be detected.
It is then diluted with acetone, whereupon the yellow acetylation product precipitates in a readily filterable form. It is filtered off, washed with acetone and the residue is heated to 40 to 50 for a short time in 5 percent soda solution in order to split off the acetyl radical that has entered the hydroxyl group. It is then salted out, filtered and dried. The resulting dye, a brown powder, dyes wool from an acid bath in orange-red tones and smoothly couples with diazo compounds. It dissolves in concentrated sulfuric acid with a blue color, while the starting dye is orange-red.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH262278T | 1946-12-20 | ||
CH267611T | 1946-12-20 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH267611A true CH267611A (en) | 1950-03-31 |
Family
ID=25730548
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH267611D CH267611A (en) | 1946-12-20 | 1946-12-20 | Process for the preparation of an oxyacylaminoazo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH267611A (en) |
-
1946
- 1946-12-20 CH CH267611D patent/CH267611A/en unknown
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