CH90860A - Process for the preparation of a green substantive trisazo dye. - Google Patents
Process for the preparation of a green substantive trisazo dye.Info
- Publication number
- CH90860A CH90860A CH90860DA CH90860A CH 90860 A CH90860 A CH 90860A CH 90860D A CH90860D A CH 90860DA CH 90860 A CH90860 A CH 90860A
- Authority
- CH
- Switzerland
- Prior art keywords
- preparation
- combined
- trisazo dye
- green
- disulfonic acid
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 4
- 238000002360 preparation method Methods 0.000 title claims description 4
- 239000002253 acid Substances 0.000 claims description 6
- 229920000742 Cotton Polymers 0.000 claims description 3
- 150000001875 compounds Chemical class 0.000 claims description 3
- 230000002378 acidificating effect Effects 0.000 claims description 2
- -1 disazo compound Chemical class 0.000 claims 1
- RUFPHBVGCFYCNW-UHFFFAOYSA-N 1-naphthylamine Chemical compound C1=CC=C2C(N)=CC=CC2=C1 RUFPHBVGCFYCNW-UHFFFAOYSA-N 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- 239000000243 solution Substances 0.000 description 3
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- PPWKNGVDZOPRPG-UHFFFAOYSA-N 3-amino-N-(8-hydroxynaphthalen-1-yl)benzamide Chemical compound NC1=CC=CC(C(=O)NC=2C3=C(O)C=CC=C3C=CC=2)=C1 PPWKNGVDZOPRPG-UHFFFAOYSA-N 0.000 description 1
- IOVCWXUNBOPUCH-UHFFFAOYSA-M Nitrite anion Chemical compound [O-]N=O IOVCWXUNBOPUCH-UHFFFAOYSA-M 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 150000008049 diazo compounds Chemical class 0.000 description 1
- QELUYTUMUWHWMC-UHFFFAOYSA-N edaravone Chemical compound O=C1CC(C)=NN1C1=CC=CC=C1 QELUYTUMUWHWMC-UHFFFAOYSA-N 0.000 description 1
- 239000013067 intermediate product Substances 0.000 description 1
- VIXWGKYSYIBATJ-UHFFFAOYSA-N pyrrol-2-one Chemical compound O=C1C=CC=N1 VIXWGKYSYIBATJ-UHFFFAOYSA-N 0.000 description 1
- 235000010288 sodium nitrite Nutrition 0.000 description 1
Landscapes
- Coloring (AREA)
Description
Verfahren zur Darstellung eines grünen substantiven Trisazofarbstoffes. Gegenstand vorliegender Erfindung ist ein Verfahren zur Darstellung eines grünen -sub- stantiven Baumwolltrisazofarbstoffes, welches darauf beruht, dass 1-Naphtalindiazo-4:
7-di- sulfosäure mit 1-Naphtylamin in saurem Medium kombiniert, das so gebildete Zwi schenprodukt weiterdiazotiert, die daraus ent stehende Diazoazoverbindung mit 1-m-Aminö- benzoylamino-8-naphtol.3 # 6-disulfosäure in al kalischem Medium kombiniert, die so erhal tene Disazoverbindung weiterdi:
izotiert und die daraus erhaltene Diazodisazoverbindung mit 1-Phenyl-3-methyl-5-pyi#azolon in alka lischem Medium kombiniert wird.
<I>Beispiel:</I> 32,5 Teile 1-Aminonaphtalin-4:7-disulfö- säure (Monoriatriumsalz) werden diazotiert und in salzsaurer Lösung mit 15 Teilen 1-Naphtylamiri kombiniert. Man lässt dann eine Lösung von 7,5 Teilen Natriumnitrit zulaufen.
Man salzt die Diazoverbindung aus, filtriert sie ab, rührt sie mit Wasser an und lässt sie unter Kühlung in eine sodaalkalische Lösung von 40 Teilen 1-m-Amiriobenzoyl- aminö-8-naphtöl-3 # 6-disulfosäurefliessen.Nach erfolgter Kombination salzt man den.
blauen Disazofarbstoff warm aus, löst ihn in Wässer und diazotiert ihn bei gewöhnlicher Tewpe- ratur in der üblichen Weise mit Salzsäure und Nitrit und nimmt die Kombination mit 7,5 Teilen 1-Phenyl-3-methyl-5-pyrazolon in sodaälkalischer Lösung bei niederer Tem peratur vor, worauf der Baumwolle grünfär bende fertige Farbstoff aasgesalzen wird.
Process for the preparation of a green substantive trisazo dye. The present invention relates to a process for the preparation of a green -sub- stantiven cotton trisazo dye, which is based on the fact that 1-naphthalene-diazo-4:
7-disulfonic acid combined with 1-naphthylamine in an acidic medium, the intermediate product formed in this way is further diazotized, the resulting diazoazo compound is combined with 1-m-aminobenzoylamino-8-naphthol.3 # 6-disulfonic acid in an alkaline medium, continue the disazo connection obtained in this way:
izotiert and the diazodisazo compound obtained therefrom is combined with 1-phenyl-3-methyl-5-pyi # azolone in an alkaline medium.
<I> Example: </I> 32.5 parts of 1-aminonaphthalene-4: 7-disulphoic acid (monoriatic salt) are diazotized and combined with 15 parts of 1-naphthylamine in a hydrochloric acid solution. A solution of 7.5 parts of sodium nitrite is then allowed to run in.
The diazo compound is salted out, filtered off, stirred with water and allowed to flow into a soda-alkaline solution of 40 parts of 1-m-amiriobenzoylamino-8-naphthoil-3 # 6-disulfonic acid while cooling. After the combination is complete, it is salted the.
warm blue disazo dye, dissolves it in water and diazotizes it at ordinary temperature in the usual way with hydrochloric acid and nitrite and takes the combination with 7.5 parts of 1-phenyl-3-methyl-5-pyrazolone in a solution of soda alkaline at lower Tem perature, whereupon the cotton green-colored finished dye is carrion salt.
Claims (1)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE89058X | 1914-06-19 | ||
| DE130715X | 1915-07-13 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH90860A true CH90860A (en) | 1921-10-01 |
Family
ID=5642586
Family Applications (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH90859D CH90859A (en) | 1914-06-19 | 1920-07-10 | Process for the preparation of a green substantive trisazo dye. |
| CH90860D CH90860A (en) | 1914-06-19 | 1920-07-10 | Process for the preparation of a green substantive trisazo dye. |
| CH89058D CH89058A (en) | 1914-06-19 | 1920-07-10 | Process for the preparation of a green substantive trisazo dye. |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH90859D CH90859A (en) | 1914-06-19 | 1920-07-10 | Process for the preparation of a green substantive trisazo dye. |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH89058D CH89058A (en) | 1914-06-19 | 1920-07-10 | Process for the preparation of a green substantive trisazo dye. |
Country Status (1)
| Country | Link |
|---|---|
| CH (3) | CH90859A (en) |
-
1920
- 1920-07-10 CH CH90859D patent/CH90859A/en unknown
- 1920-07-10 CH CH90860D patent/CH90860A/en unknown
- 1920-07-10 CH CH89058D patent/CH89058A/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| CH89058A (en) | 1921-04-16 |
| CH90859A (en) | 1921-10-01 |
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