CH262170A - Process for the preparation of a brown polyazo dye. - Google Patents
Process for the preparation of a brown polyazo dye.Info
- Publication number
- CH262170A CH262170A CH262170DA CH262170A CH 262170 A CH262170 A CH 262170A CH 262170D A CH262170D A CH 262170DA CH 262170 A CH262170 A CH 262170A
- Authority
- CH
- Switzerland
- Prior art keywords
- mole
- brown
- dye
- mol
- 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
- C09B35/00—Disazo and polyazo dyes of the type A<-D->B prepared by diazotising and coupling
- C09B35/38—Trisazo dyes ot the type
- C09B35/40—Trisazo dyes ot the type the component K being a dihydroxy or polyhydroxy compound
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
<B>Zusatzpatent</B> zum Hauptpatent Nr. 255411. Verfahren zur Herstellung eines braunen Polyazofarbstoffes. Das vorliegende Patent betrifft ein Ver fahren zur Herstellung eines braunen Poly- azofarbstoffes und ist dadurch gekennzeich net, dass man 1 Mol Resorcin, 1 Mol der Ver bindung,
erhältlich durch Verseifen und Di- azotieren des Farbstoffes aus 1 Mol diazotier- ter Naphthionsäure und 1 Mol 1-Methyl-3- acetamino-4-oxybenzol, und 1 Mol der aus 1 Mol tetrazotiertem Benzidin und 1 Mol Sali- zylsäure erhältlichen Zwischenverbindung aufeinander einwirken lässt.
.Beispiel: Man vereinigt eine wie üblich hergestellte Diazoverbindung von 22,3g Naphthionsäure mit einer Lösung von 16,5 g 1-Methyl-3-acet- amino-4-oxybenzol, 13,3 g 30%iger Natron lauge und Wasser in Gegenwart von Soda. Der Monoazofarbstoff wird mit Kochsalz ab geschieden und durch mehrstündiges Erwär men mit verdünnter Schwefelsäure verseift. Nach Erkalten wird der Monoazofarbstoff, der die mutmassliche Formel
EMI0001.0030
besitzt, filtriert und mit Wasser ausgewa schen.
Er wird in Wasser und Natronlauge gelöst, mit 7 g Natriumnitrit versetzt und un ter gutem Rühren bei niedriger Temperatur in Salzsäure eingetropft. Nach beendeter Di- a.zotierung kuppelt man mit einer sodaalkali- schen Lösung von 11g Resorcin. Der Disazo- farbstoff wird durch Zusatz von Salzsäure abgeschieden. Er wird in Soda und Wasser gelöst und mit der wie üblich hergestellten Zwischenverbindung aus 18,4 g Benzidin und 13,8 g Salizylsäure gekuppelt.
Der Tetrakis- azofarbstoff wird in der Wärme mit Kochsalz abgeschieden. Er stellt ein dunkles Pulver dar und färbt Baumwolle in rotbraunen Tönen, die nach Behandlung mit Kupfersalzen braun werden. Die Wasch-, Licht- und Alkalieclit- lieiten werden dabei erheblich verbessert.
<B> Additional patent </B> to main patent no. 255411. Process for the production of a brown polyazo dye. The present patent relates to a process for the production of a brown poly azo dye and is characterized in that 1 mole of resorcinol, 1 mole of the compound,
obtainable by saponifying and diazotizing the dye from 1 mole of diazotized naphthionic acid and 1 mole of 1-methyl-3-acetamino-4-oxybenzene, and 1 mole of the intermediate compound obtainable from 1 mole of tetrazotized benzidine and 1 mole of salicylic acid interact leaves.
Example: A conventionally prepared diazo compound of 22.3 g of naphthionic acid is combined with a solution of 16.5 g of 1-methyl-3-acetamino-4-oxybenzene, 13.3 g of 30% strength sodium hydroxide solution and water in the presence of soda. The monoazo dye is separated with common salt and saponified with dilute sulfuric acid by heating for several hours. After cooling down, the monoazo dye, which has the presumed formula
EMI0001.0030
owns, filtered and washed out with water.
It is dissolved in water and sodium hydroxide solution, 7 g of sodium nitrite are added and the mixture is added dropwise to hydrochloric acid at low temperature, stirring thoroughly. After the end of the dipoting, coupling is carried out with a soda-alkaline solution of 11 g of resorcinol. The disazo dye is deposited by adding hydrochloric acid. It is dissolved in soda and water and coupled with the intermediate compound prepared as usual from 18.4 g of benzidine and 13.8 g of salicylic acid.
The tetrakis azo dye is deposited in the heat with common salt. It is a dark powder and dyes cotton in red-brown tones, which turn brown after treatment with copper salts. The wash, light and alkali class are considerably improved.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH262170T | 1943-07-02 | ||
CH255411T | 1948-06-30 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH262170A true CH262170A (en) | 1949-06-15 |
Family
ID=25729898
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH262170D CH262170A (en) | 1943-07-02 | 1943-07-02 | Process for the preparation of a brown polyazo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH262170A (en) |
-
1943
- 1943-07-02 CH CH262170D patent/CH262170A/en unknown
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CH262170A (en) | Process for the preparation of a brown polyazo dye. | |
DE870883C (en) | Process for the production of mono-, dis- and polyazo dyes | |
CH262168A (en) | Process for the preparation of a brown polyazo dye. | |
CH262171A (en) | Process for the preparation of a brown polyazo dye. | |
AT101312B (en) | Process for the preparation of substantive cotton dyes. | |
AT40668B (en) | Process for the preparation of trisazo dyes. | |
CH246188A (en) | Process for the production of a metallizable polyazo dye. | |
DE928903C (en) | Process for the preparation of monoazo dyes | |
DE815513C (en) | Process for the preparation of disazo or polyazo dyes | |
CH246185A (en) | Process for the production of a metallizable polyazo dye. | |
CH246186A (en) | Process for the production of a metallizable polyazo dye. | |
AT37561B (en) | Process for the preparation of secondary disazo dyes. | |
CH262172A (en) | Process for the preparation of a brown polyazo dye. | |
CH246189A (en) | Process for the production of a metallizable polyazo dye. | |
CH262167A (en) | Process for the preparation of a brown polyazo dye. | |
CH148005A (en) | Process for the preparation of a disazo dye. | |
CH249553A (en) | Process for the preparation of a polyazo dye. | |
CH209562A (en) | Process for the preparation of a polyazo dye. | |
CH217952A (en) | Process for the preparation of a disazo dye. | |
CH183457A (en) | Process for the preparation of a new trisazo dye. | |
CH246187A (en) | Process for the production of a metallizable polyazo dye. | |
CH282092A (en) | Process for the preparation of a copper-compatible tetrakisazo dye. | |
CH185945A (en) | Process for the preparation of an azo dye. | |
CH202733A (en) | Process for the preparation of an azo dye. | |
CH212995A (en) | Process for the preparation of a hexakisazo dye. |