CH214545A - Process for the preparation of an azo dye. - Google Patents
Process for the preparation of an azo dye.Info
- Publication number
- CH214545A CH214545A CH214545DA CH214545A CH 214545 A CH214545 A CH 214545A CH 214545D A CH214545D A CH 214545DA CH 214545 A CH214545 A CH 214545A
- Authority
- CH
- Switzerland
- Prior art keywords
- red
- azo dye
- tones
- preparation
- oxybenzene
- Prior art date
Links
- 239000000987 azo dye Substances 0.000 title claims description 4
- 238000000034 method Methods 0.000 title claims description 4
- 238000002360 preparation method Methods 0.000 title description 2
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 claims description 6
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims description 6
- 239000000975 dye Substances 0.000 claims description 5
- 229910000029 sodium carbonate Inorganic materials 0.000 claims description 3
- 239000002253 acid Substances 0.000 claims description 2
- 150000007513 acids Chemical class 0.000 claims description 2
- 150000008049 diazo compounds Chemical class 0.000 claims description 2
- RIFGWPKJUGCATF-UHFFFAOYSA-N ethyl chloroformate Chemical compound CCOC(Cl)=O RIFGWPKJUGCATF-UHFFFAOYSA-N 0.000 claims description 2
- 238000009963 fulling Methods 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims description 2
- 238000004382 potting Methods 0.000 claims description 2
- 239000000843 powder Substances 0.000 claims description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 2
- 210000002268 wool Anatomy 0.000 claims description 2
- 239000000243 solution Substances 0.000 description 3
- 230000008878 coupling Effects 0.000 description 2
- 238000010168 coupling process Methods 0.000 description 2
- 238000005859 coupling reaction Methods 0.000 description 2
- 230000010933 acylation Effects 0.000 description 1
- 238000005917 acylation reaction Methods 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
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
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05K—PRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
- H05K2201/00—Indexing scheme relating to printed circuits covered by H05K1/00
- H05K2201/09—Shape and layout
- H05K2201/09209—Shape and layout details of conductors
- H05K2201/09654—Shape and layout details of conductors covering at least two types of conductors provided for in H05K2201/09218 - H05K2201/095
- H05K2201/09809—Coaxial layout
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05K—PRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
- H05K2201/00—Indexing scheme relating to printed circuits covered by H05K1/00
- H05K2201/10—Details of components or other objects attached to or integrated in a printed circuit board
- H05K2201/10007—Types of components
- H05K2201/10196—Variable component, e.g. variable resistor
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
Verfahren zur Herstellung eines Azofarbstoffes. Vorliegendes Patent bezieht sich auf ein Verfahren zur Herstellung eines Azofarbstoffes, dadurch gekennzeichnet, dass man die Diazo- verbindung von 6-Chlor-2-amino-l-oxybenzol mit dem Einwirkungsprodukt von 1 Mol. Chlorkohlensäureäthylester und 1 Mol. Essig säureanhydrid auf 1. 5-Diamino-3-oxynaphtha- lin-7-sulfonsäure vereinigt.
Der Farbstoff ist getrocknet ein dunkles Pulver, das sich in verdünnten Säuren mit roter, in Natriumcarbonatlösung mit blauer und in konzentrierter Schwefelsäure mit blau stichig-roter Farbe löst, und färbt Wolle in roten Tönen, die beim Ohromieren in rot stichig-graue Töne von sehr guter Licht-, Walk-, Carbonisier- und Pottingechtheit über gehen.
Beispiel: 14,3 Gewichtsteile 6-Chlor-2-amino-l-oxy- benzol werden diazotiert. Die Diazolösung lässt man in eine überschüssiges Natrium- carbonat enthaltende Lösung von 37 Gewichts teilen einer Kupplungskomponente einlaufen, die man erhält, wenn man 25,4 Gewichtst 1e 1 .
5 -Diamino - 3 - oxynaphthalin- 7 - sulfonsäure nacheinander mit 11 Gewichtsteilen Chlor- kohensäureäthylester und dann bis zur Be endigung der Acylierung mit Essigsäure- anhydridinwässerigerLösung behandelt. Nach beendeter Kupplung wird der Farbstoff ab geschieden und getrocknet.
Process for the preparation of an azo dye. The present patent relates to a process for the production of an azo dye, characterized in that the diazo compound of 6-chloro-2-amino-1-oxybenzene is mixed with the action product of 1 mol. Of ethyl chlorocarbonate and 1 mol. Of acetic anhydride to 1. 5-diamino-3-oxynaphthalin-7-sulfonic acid combined.
The dyestuff is a dried dark powder that dissolves in dilute acids with red, in sodium carbonate solution with blue and in concentrated sulfuric acid with bluish-red color, and it dyes wool in red tones, which when odorized in red, cast-gray tones of very good fastness to light, fulling, carbonising and potting.
Example: 14.3 parts by weight of 6-chloro-2-amino-1-oxybenzene are diazotized. The diazo solution is allowed to run into a solution of 37 parts by weight of a coupling component which contains excess sodium carbonate and which is obtained when 25.4 parts by weight of 1e 1.
Treated 5-diamino-3-oxynaphthalene-7-sulfonic acid in succession with 11 parts by weight of ethyl chloroate and then with acetic anhydridine aqueous solution until the acylation is complete. After the coupling has ended, the dye is separated off and dried.
Claims (1)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE214545X | 1938-05-21 | ||
| CH212417T | 1939-04-25 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH214545A true CH214545A (en) | 1941-04-30 |
Family
ID=25725231
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH214545D CH214545A (en) | 1938-05-21 | 1939-04-25 | Process for the preparation of an azo dye. |
Country Status (1)
| Country | Link |
|---|---|
| CH (1) | CH214545A (en) |
-
1939
- 1939-04-25 CH CH214545D patent/CH214545A/en unknown
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