CH194084A - Process for the preparation of an o-oxyazo dye. - Google Patents
Process for the preparation of an o-oxyazo dye.Info
- Publication number
- CH194084A CH194084A CH194084DA CH194084A CH 194084 A CH194084 A CH 194084A CH 194084D A CH194084D A CH 194084DA CH 194084 A CH194084 A CH 194084A
- Authority
- CH
- Switzerland
- Prior art keywords
- dye
- preparation
- green
- oxyazo
- dyeings
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 3
- 239000000975 dye Substances 0.000 claims description 6
- 238000004043 dyeing Methods 0.000 claims description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 3
- ZYECOAILUNWEAL-NUDFZHEQSA-N (4z)-4-[[2-methoxy-5-(phenylcarbamoyl)phenyl]hydrazinylidene]-n-(3-nitrophenyl)-3-oxonaphthalene-2-carboxamide Chemical compound COC1=CC=C(C(=O)NC=2C=CC=CC=2)C=C1N\N=C(C1=CC=CC=C1C=1)/C(=O)C=1C(=O)NC1=CC=CC([N+]([O-])=O)=C1 ZYECOAILUNWEAL-NUDFZHEQSA-N 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
- 230000002378 acidificating effect Effects 0.000 claims 2
- 239000000987 azo dye Substances 0.000 claims 1
- 239000002253 acid Substances 0.000 description 4
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- 230000008878 coupling Effects 0.000 description 2
- 238000010168 coupling process Methods 0.000 description 2
- 238000005859 coupling reaction Methods 0.000 description 2
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 1
- 238000004532 chromating Methods 0.000 description 1
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
Landscapes
- Coloring (AREA)
Description
Verfahren zur Darstellung eines o-Ogyazofarbstoffes. Es wurde gefunden, dass durch Kuppeln von dianotiertem 5-Nitro-2-amino-l-oxybenzol mit 2-Phenylamino-6-oxynaphtbalin-8-sulfoii- säure ein Farbstoff erhalten wird, der durch Nachchromieren der in saurem Bade ent stehenden Färbungen gleichmässige, graue Färbungen von ausgezeichneten Echtheits eigenschaften liefert. <I>Beispiel:</I> 15,4 kg 5-Nitro-2-amino-l-oxybenzol wer den in üblicher Weise dianotiert.
Die Diazo- lösung, deren Mineralsäure mit Natriumbi- carbonat abgestumpft wird, fliesst zu einer Lösung von 31,5 kg 2-Phenylamino-6-oxy- naphthalin-8-sulfonsäure, hergestellt in be kannter Weise durch Phenylieren von 2- Amino-6-oxynaphthalin-8-sulfonsäure, in 250 Liter Wasser, 10 kg Natriumbicarbonat und 100 Liter Pyridin.
Nach beendeter Kupplung wird filtriert. Der Farbstoff, ein dunkles Pulver, löst sich in Wasser grün und in konzentrierter Schwe- felsäure rotviolett. Er färbt Wolle aus saurem Bade grün. Beim Nachchromieren der Färbung erhält man ein lichtechtes Grau.
Process for the preparation of an o-ogyazo dye. It has been found that by coupling dianotized 5-nitro-2-amino-1-oxybenzene with 2-phenylamino-6-oxynaphthalene-8-sulfoic acid, a dye is obtained which is uniform by after-chromating the colorations that arise in an acid bath , provides gray dyeings with excellent fastness properties. <I> Example: </I> 15.4 kg of 5-nitro-2-amino-1-oxybenzene are dianotized in the usual way.
The diazo solution, the mineral acid of which is truncated with sodium bicarbonate, flows into a solution of 31.5 kg of 2-phenylamino-6-oxynaphthalene-8-sulfonic acid, prepared in a known manner by phenylating 2-amino-6 -oxynaphthalene-8-sulfonic acid, in 250 liters of water, 10 kg of sodium bicarbonate and 100 liters of pyridine.
After the coupling has ended, it is filtered. The dye, a dark powder, dissolves green in water and red-violet in concentrated sulfuric acid. He dyes wool from acid bath green. When the color is re-chromed, a lightfast gray is obtained.
Claims (1)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH184880T | 1935-08-24 | ||
| DE194084X | 1936-05-06 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH194084A true CH194084A (en) | 1937-11-15 |
Family
ID=25721108
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH194084D CH194084A (en) | 1935-08-24 | 1937-01-05 | Process for the preparation of an o-oxyazo dye. |
Country Status (1)
| Country | Link |
|---|---|
| CH (1) | CH194084A (en) |
-
1937
- 1937-01-05 CH CH194084D patent/CH194084A/en unknown
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