CH209095A - Process for the preparation of a monoazo dye. - Google Patents
Process for the preparation of a monoazo dye.Info
- Publication number
- CH209095A CH209095A CH209095DA CH209095A CH 209095 A CH209095 A CH 209095A CH 209095D A CH209095D A CH 209095DA CH 209095 A CH209095 A CH 209095A
- Authority
- CH
- Switzerland
- Prior art keywords
- preparation
- monoazo dye
- dye
- silk
- yellow
- Prior art date
Links
- NYGZLYXAPMMJTE-UHFFFAOYSA-M metanil yellow Chemical group [Na+].[O-]S(=O)(=O)C1=CC=CC(N=NC=2C=CC(NC=3C=CC=CC=3)=CC=2)=C1 NYGZLYXAPMMJTE-UHFFFAOYSA-M 0.000 title claims description 4
- 238000000034 method Methods 0.000 title claims description 4
- 239000000975 dye Substances 0.000 claims description 7
- LUZXGSRCYGQGQF-UHFFFAOYSA-N 2,5-dichloro-4-(5-methyl-3-oxo-1h-pyrazol-2-yl)benzenesulfonic acid Chemical compound N1C(C)=CC(=O)N1C1=CC(Cl)=C(S(O)(=O)=O)C=C1Cl LUZXGSRCYGQGQF-UHFFFAOYSA-N 0.000 claims description 2
- 238000004043 dyeing Methods 0.000 claims description 2
- 230000007935 neutral effect Effects 0.000 claims description 2
- 239000000843 powder Substances 0.000 claims description 2
- 210000002268 wool Anatomy 0.000 claims description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- KCEIVWKDBLAQKL-UHFFFAOYSA-N 2,5-dichloro-4-(3-methyl-5-oxo-4h-pyrazol-1-yl)benzenesulfonic acid Chemical compound O=C1CC(C)=NN1C1=CC(Cl)=C(S(O)(=O)=O)C=C1Cl KCEIVWKDBLAQKL-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
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
- C09B29/00—Monoazo dyes prepared by diazotising and coupling
- C09B29/34—Monoazo dyes prepared by diazotising and coupling from other coupling components
- C09B29/36—Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds
- C09B29/3604—Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds containing only a nitrogen as heteroatom
- C09B29/3647—Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds containing only a nitrogen as heteroatom containing a five-membered ring with two nitrogen atoms as heteroatoms
- C09B29/3652—Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds containing only a nitrogen as heteroatom containing a five-membered ring with two nitrogen atoms as heteroatoms containing a 1,2-diazoles or hydrogenated 1,2-diazoles
- C09B29/366—Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds containing only a nitrogen as heteroatom containing a five-membered ring with two nitrogen atoms as heteroatoms containing a 1,2-diazoles or hydrogenated 1,2-diazoles containing hydroxy-1,2-diazoles, e.g. pyrazolone
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
Verfahren zur Darstellung eines Monoazofarbstoffes. Das vorliegende Patent betrifft ein Ver fahren zur Darstellung eines Monoazofarb- stoffes und ist dadurch gekennzeichnet, dass man 4 - (4' - Chlorbenzyl - 2" - chlorbenzoyl)- amino-l-aminobenzol diazotiert und mit 1 (2',5'-Dichlor-4'-sulfophenyl)-3-methyl-5-pyr- azolon kuppelt.
Beispiel: 37,1 Teile 4-(4'-Chlorbenzyl-2"-chlorben- zoyl) -amino-l-aminobenzol werden mit 6,9 Tei len Nitrit und 25 Teilen Salzsäure diazotiert und in Gegenwart von Soda mit 32,3 Teilen 1- (2', 5' -Dichlor- 4' - sulf ophenyl)- 3-methyl-5- pyrazolon gekuppelt. Der isolierte und ge trocknete Farbstoff stellt ein gelbes Pulver dar und färbt Wolle und Seide licht-, walk- und schweissecht lebhaft gelb. Er eignet sich vorzüglich zum Färben von Seide aus neu tralem Bad.
Process for the preparation of a monoazo dye. The present patent relates to a process for the preparation of a monoazo dye and is characterized in that 4 - (4 '- chlorobenzyl - 2 "- chlorobenzoyl) - amino-1-aminobenzene is diazotized and 1 (2', 5'- Dichloro-4'-sulfophenyl) -3-methyl-5-pyr-azolone couples.
Example: 37.1 parts of 4- (4'-chlorobenzyl-2 "-chlorobenzoyl) -amino-1-aminobenzene are diazotized with 6.9 parts of nitrite and 25 parts of hydrochloric acid and in the presence of soda with 32.3 parts 1- (2 ', 5' -Dichlor- 4 '- sulfophenyl) - 3-methyl-5-pyrazolone coupled.The isolated and dried dye is a yellow powder and dyes wool and silk fast to light, milled and perspiration lively yellow, it is ideal for dyeing silk from neutral baths.
Claims (1)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH209095T | 1938-03-02 | ||
| CH203692T | 1938-03-02 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH209095A true CH209095A (en) | 1940-03-15 |
Family
ID=25723960
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH209095D CH209095A (en) | 1938-03-02 | 1938-03-02 | Process for the preparation of a monoazo dye. |
Country Status (1)
| Country | Link |
|---|---|
| CH (1) | CH209095A (en) |
-
1938
- 1938-03-02 CH CH209095D patent/CH209095A/en unknown
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