CH185844A - Process for the preparation of an azo dye. - Google Patents
Process for the preparation of an azo dye.Info
- Publication number
- CH185844A CH185844A CH185844DA CH185844A CH 185844 A CH185844 A CH 185844A CH 185844D A CH185844D A CH 185844DA CH 185844 A CH185844 A CH 185844A
- Authority
- CH
- Switzerland
- Prior art keywords
- dye
- azo dye
- preparation
- aminobenzene
- methoxy
- Prior art date
Links
- 239000000987 azo dye Substances 0.000 title claims description 4
- 238000000034 method Methods 0.000 title claims description 3
- 238000002360 preparation method Methods 0.000 title description 2
- 239000000975 dye Substances 0.000 claims description 7
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims description 6
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 4
- 239000000654 additive Substances 0.000 claims description 3
- WXWCDTXEKCVRRO-UHFFFAOYSA-N para-Cresidine Chemical compound COC1=CC=C(C)C=C1N WXWCDTXEKCVRRO-UHFFFAOYSA-N 0.000 claims description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims description 2
- 239000003960 organic solvent Substances 0.000 claims description 2
- 239000000843 powder Substances 0.000 claims description 2
- 230000002378 acidificating effect Effects 0.000 claims 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- 239000002253 acid Substances 0.000 description 2
- LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 1
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 235000010288 sodium nitrite Nutrition 0.000 description 1
- 238000003756 stirring Methods 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
- C09B29/06—Monoazo dyes prepared by diazotising and coupling from coupling components containing amino as the only directing group
- C09B29/08—Amino benzenes
- C09B29/0805—Amino benzenes free of acid groups
- C09B29/0807—Amino benzenes free of acid groups characterised by the amino group
- C09B29/0808—Amino benzenes free of acid groups characterised by the amino group unsubstituted amino group
-
- 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
- C09B29/06—Monoazo dyes prepared by diazotising and coupling from coupling components containing amino as the only directing group
- C09B29/08—Amino benzenes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
- Paper (AREA)
Description
Verfahren zur Herstellung eines Azofarbstoffes. Es wurde gefunden, dass man einen Azo- farbstoff erhält, wenn man diazotiertes 1- Aminobenzol-4-methylsulfon in saurem. Me dium mit 1-Amino-2-methoxy-5-methylben- zol vereinigt.
Der so erhältliche Farbstoff bildet ein gelbrotes Pulver, das sich in organischen Lösungsmitteln, wie Aceton, Essigester usw., mit oranger Farbe löst. Durch geeignete Zusätze in feine Verteilung gebracht, färbt der Farbstoff Acetatseide in echten orangen Tönen.
<I>Beispiel:</I> <B>171</B> Teile 1-Aminobenzol-4-methylsulfon werden in salzsaurer Lösung in üblicher Weise mit 69 Teilen. Natriumnitrit diazotiert. Zu der Diazolösung lässt man eine wässerige Lösung von 137 Teilen 1-Amino-2-methoxy- 5-methylbenzol und der erforderlichen Menge Salzsäure zutropfen. Man rührt, bis die Kupplung,
die man gegebenenfalls durch sorgfältige Zugabe säurebindender oder ab stumpfender Zusätze beschleunigt, beendet ist. Hierauf wird der Farbstoff filtriert, neutral .gewaschen und getrocknet.
Process for the preparation of an azo dye. It has been found that an azo dye is obtained when diazotized 1-aminobenzene-4-methylsulfone is dissolved in acid. Medium combined with 1-amino-2-methoxy-5-methylben- zene.
The dye thus obtainable forms a yellow-red powder that dissolves in organic solvents such as acetone, ethyl acetate, etc., with an orange color. Finely dispersed by suitable additives, the dye acetate silk dyes in real orange tones.
<I> Example: </I> <B> 171 </B> parts of 1-aminobenzene-4-methylsulfone are used in hydrochloric acid solution in the usual way with 69 parts. Sodium nitrite diazotized. An aqueous solution of 137 parts of 1-amino-2-methoxy-5-methylbenzene and the required amount of hydrochloric acid are added dropwise to the diazo solution. Stir until the clutch
which is optionally accelerated by careful addition of acid-binding or blunt additives, has ended. The dye is then filtered, washed until neutral and dried.
Claims (1)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH185844T | 1935-01-29 | ||
| CH183204T | 1935-01-29 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH185844A true CH185844A (en) | 1936-08-15 |
Family
ID=25720849
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH185844D CH185844A (en) | 1935-01-29 | 1935-01-29 | Process for the preparation of an azo dye. |
Country Status (1)
| Country | Link |
|---|---|
| CH (1) | CH185844A (en) |
-
1935
- 1935-01-29 CH CH185844D patent/CH185844A/en unknown
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