CH218810A - Process for the preparation of a monoazo dye. - Google Patents
Process for the preparation of a monoazo dye.Info
- Publication number
- CH218810A CH218810A CH218810DA CH218810A CH 218810 A CH218810 A CH 218810A CH 218810D A CH218810D A CH 218810DA CH 218810 A CH218810 A CH 218810A
- Authority
- CH
- Switzerland
- Prior art keywords
- preparation
- amino
- monoazo dye
- dye
- oxynaphthoyl
- Prior art date
Links
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
- C09B29/10—Monoazo dyes prepared by diazotising and coupling from coupling components containing hydroxy as the only directing group
- C09B29/18—Monoazo dyes prepared by diazotising and coupling from coupling components containing hydroxy as the only directing group ortho-Hydroxy carbonamides
- C09B29/20—Monoazo dyes prepared by diazotising and coupling from coupling components containing hydroxy as the only directing group ortho-Hydroxy carbonamides of the naphthalene series
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
Verfahren zur Herstellung eines Nonoazofarbstoffes. Gegenstand des vorliegenden Zusatzpa tentes ist ein Verfahren zur Herstellung eines Monoazofarbstoffes, welches dadurch gekenn zeichnet ist, dass man die Diazoverbindung von 1-Amino-2,5-dimethoxybenzol-4-(sulfonyl- n- dibutylamin) mit 2,3 - Oxynaphthoyl- (1'- amino-4'-methoxybenzol) kuppelt.
<I>Beispiel:</I> 34,4 Gewichtsteile 1-Amino-2,5-dimethoxy- benzol-4-(sulfonyl-n-dibutylamin) werden, wie üblich, diazotiert. Die mit Natriumacetat auf Kongoneutralität abgestumpfte Diazolösung rührt man in eine Lösung von 29,3 Gewichts teilen 2,3-Oxynaphthoyl-(1'-amino-4'-methoxy- benzol) in verdünnter Natronlauge ein. Der entstehende Farbstoff wird abfiltriert, gut ausgewaschen und getrocknet.
Er stellt ein bordorotes Pulver dar, das in Butylalkohol, Essigester, Benzol und an dern organischen Lösungsmitteln gut löslich ist und Celluloseesterlacke, wie auch Kerzen und Fette, in bordoroten Tönen von guten Echtheitseigenschaften färbt.
Process for the preparation of a nonoazo dye. The subject of the present additional patent is a process for the production of a monoazo dye, which is characterized in that the diazo compound of 1-amino-2,5-dimethoxybenzene-4- (sulfonyl- n-dibutylamine) with 2,3 - oxynaphthoyl- (1'-amino-4'-methoxybenzene) couples.
<I> Example: </I> 34.4 parts by weight of 1-amino-2,5-dimethoxybenzene-4- (sulfonyl-n-dibutylamine) are diazotized as usual. The diazo solution, truncated to Congo neutrality with sodium acetate, is stirred into a solution of 29.3 parts by weight of 2,3-oxynaphthoyl- (1'-amino-4'-methoxybenzene) in dilute sodium hydroxide solution. The resulting dye is filtered off, washed well and dried.
It is a red powder that is readily soluble in butyl alcohol, ethyl acetate, benzene and other organic solvents and colors cellulose ester lacquers, as well as candles and fats, in red shades with good fastness properties.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE218810X | 1938-09-15 | ||
CH214172T | 1939-09-07 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH218810A true CH218810A (en) | 1941-12-31 |
Family
ID=25725541
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH218810D CH218810A (en) | 1938-09-15 | 1939-09-07 | Process for the preparation of a monoazo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH218810A (en) |
-
1939
- 1939-09-07 CH CH218810D patent/CH218810A/en unknown
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