CH98021A - Process for the preparation of an o-oxymonoazo dye. - Google Patents
Process for the preparation of an o-oxymonoazo dye.Info
- Publication number
- CH98021A CH98021A CH98021DA CH98021A CH 98021 A CH98021 A CH 98021A CH 98021D A CH98021D A CH 98021DA CH 98021 A CH98021 A CH 98021A
- Authority
- CH
- Switzerland
- Prior art keywords
- dye
- oxymonoazo
- preparation
- oxybenzene
- formylamino
- 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
- C09B29/24—Monoazo dyes prepared by diazotising and coupling from coupling components containing both hydroxyl and amino directing groups
- C09B29/26—Amino phenols
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Darstellung eines o-Oxymonoazofarbstoffes. Im Hauptpatent wurde die Darstellung eines Farbstoffes beschrieben, der mit Hilfe von Chrombeizen auf Wolle olive farbige Töne von hervorragender Wasch-; Walk-. Potting- und Lichtechtheit erzeugt. Der Farb stoff wird dargestellt durch Kupplung von dianotierter Piliraminsäure mit 4-Acetyl- aminophenol.
In diesem Verfahren lässt sich mit glei chem Erfolg das 4-Acetylaminopheriol durch 1. - DZethyl-3-formylamino-4-oxybenzol erset zen.
Beispiel: 19,9 Teile Pikraminsäure werden, wie üblich, dianotiert und mit einer sodaalkali- schen Lösung von 15,1 Teilen 1-Methyl-3- formylamino-4-oxybenzol vereinigt. Der fer tig gebildete Farbstoff wird ausgesalzen und abgepresst. Er bildet getrocknet ein schwärz- liches Pulver, das sich in heissem Wasser orange löst.
Process for the preparation of an o-oxymonoazo dye. In the main patent, the representation of a dye was described, with the help of chrome stains on wool olive tones of excellent washing; Walk-. Potting and lightfastness generated. The dye is produced by coupling dianotated piliramic acid with 4-acetylaminophenol.
In this process, the 4-acetylaminopheriol can be replaced by 1.-DZethyl-3-formylamino-4-oxybenzene with the same success.
Example: 19.9 parts of picric acid are dianotized as usual and combined with a soda-alkaline solution of 15.1 parts of 1-methyl-3-formylamino-4-oxybenzene. The finished dye is salted out and pressed out. When dried, it forms a blackish powder that dissolves orange in hot water.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH72055T | 1921-09-10 | ||
CH98021T | 1921-09-10 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH98021A true CH98021A (en) | 1923-02-16 |
Family
ID=25700946
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH98021D CH98021A (en) | 1921-09-10 | 1921-09-10 | Process for the preparation of an o-oxymonoazo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH98021A (en) |
-
1921
- 1921-09-10 CH CH98021D patent/CH98021A/en unknown
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