CH293867A - Process for the preparation of a copper-compatible polyazo dye. - Google Patents
Process for the preparation of a copper-compatible polyazo dye.Info
- Publication number
- CH293867A CH293867A CH293867DA CH293867A CH 293867 A CH293867 A CH 293867A CH 293867D A CH293867D A CH 293867DA CH 293867 A CH293867 A CH 293867A
- Authority
- CH
- Switzerland
- Prior art keywords
- mol
- copper
- oxy
- amino
- acid
- 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
- 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
- C09B35/28—Disazo dyes characterised by the tetrazo component the tetrazo component containing two aryl nuclei linked by at least one of the groups —CON<, —SO2N<, —SO2—, or —SO2—O—
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
Zusatzpatent zum Hauptpatent Nr. <B>261125.</B> Verfahren zur Herstellung eines kupferbaren Polyazofarbstoffes. Gegenstand vorliegenden Patentes ist ein Verfahren zur Herstellung eines kupferbaren Polyazofarbstoffes. Das Verfahren ist da durch gekennzeichnet, dass man<B>1</B> Mol der Tetrazoverbindung von 1-(3'-Amino-4'-oxy- benzoylamino)
<B>-</B> 4<B>-</B> amino <B>-</B> benzol-3-earbonsäure einerseits mit<B>1</B> Mol 2-(4'-Oxy-3'-earboxy- phenylamino) <B>- 5</B> -oxy-naphthalin-7-sulionsäure und anderseits mit<B>1</B> Mol 2-Methoxy-acetessig. säureanilid kuppelt.
Der erhaltene neue Disazofarbstoff stellt ein braunsehwarzes Pulver dar, das sieh in Wasser mit violettstichig roter und in konz. Schwefelsäure mit weinroter Farbe löst und Zellulosefasern in braunen Tönen anfnrbt, welche durch Nachbehandlung mit Kupfer salzen sehr gute Gesamteehtheiten aufweisen.
<I>Beispiel:</I> <B>28,7</B> Teile 1-(3'-Amino-4-oxy-benzoyl- amino)-4-amino-benzol-3-earbonsäure werden in 400 Teilen Wasser mit<B>8</B> Teilen Natron lauge kalt gelöst, mit<B>13,8</B> Teilen Natrium- nitrit vermischt und in der Kälte unter Rüh ren auf 40 Teile konz. Salzsäure und<B>80</B> Teile Wasser aufgetropft und die überschüssige Mineralsäure mit Soda abgestumpft.
Die er haltene Tetrazoverbindung wird mit<B>3,7,5</B> Tei len 2-(4'-Oxy-3'-earboxy-phenylamino)-5-oxy- naphthalin-7-sullonsäure, gelöst in<B>300</B> Teilen Wasser bei Gegenwart von 20 Teilen Soda, zum einseitigen Zwischenprodukt und nach beendigter Kupplung mit<B>20,7</B> Teilen 2-Me- thoxy-aeetessigsäureanilid und einem weiteren Zusatz von<B>5</B> Teilen Soda zum Disazofarbstoff vereinigt. Der erhaltene Farbstoff der Formel
EMI0001.0037
wird mit Kochsalz gefällt, abfiltriert und ge trocknet.
Additional patent to main patent no. <B> 261125. </B> Process for the production of a copperable polyazo dye. The present patent relates to a process for the preparation of a copperable polyazo dye. The process is characterized in that <B> 1 </B> mol of the tetrazo compound of 1- (3'-amino-4'-oxy-benzoylamino)
<B> - </B> 4 <B> - </B> amino <B> - </B> benzene-3-carboxylic acid on the one hand with <B> 1 </B> mol 2- (4'-oxy- 3'-earboxy-phenylamino) -5-oxy-naphthalene-7-sulionic acid and on the other hand with 1 mol of 2-methoxy-acetic acid. acid anilide coupling.
The new disazo dye obtained is a brownish-black powder, which looks red in water with purple tinges and in conc. Sulfuric acid with a wine-red color dissolves and stains cellulose fibers in brown tones, which after treatment with copper salts show very good overall strength.
<I> Example: </I> <B> 28.7 </B> parts of 1- (3'-amino-4-oxy-benzoyl-amino) -4-aminobenzene-3-carboxylic acid are in 400 parts Water with <B> 8 </B> parts of cold sodium hydroxide solution, mixed with <B> 13.8 </B> parts of sodium nitrite and concentrated in the cold with stirring to 40 parts. Hydrochloric acid and <B> 80 </B> parts of water are added dropwise and the excess mineral acid is blunted with soda.
The tetrazo compound obtained is mixed with 3.7.5 parts of 2- (4'-oxy-3'-earboxy-phenylamino) -5-oxynaphthalene-7-sullonic acid, dissolved in > 300 parts of water in the presence of 20 parts of soda to the one-sided intermediate product and, after coupling is complete, with 20.7 parts of 2-methoxy-aeetacetic anilide and a further addition of 5 Parts of soda combined to disazo dye. The obtained dye of the formula
EMI0001.0037
is precipitated with table salt, filtered off and dried ge.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH293867T | 1948-08-06 | ||
CH261125T | 1948-08-06 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH293867A true CH293867A (en) | 1953-10-15 |
Family
ID=25730381
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH293867D CH293867A (en) | 1948-08-06 | 1948-08-06 | Process for the preparation of a copper-compatible polyazo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH293867A (en) |
-
1948
- 1948-08-06 CH CH293867D patent/CH293867A/en unknown
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