CH195530A - Process for the preparation of a monoazo dye. - Google Patents
Process for the preparation of a monoazo dye.Info
- Publication number
- CH195530A CH195530A CH195530DA CH195530A CH 195530 A CH195530 A CH 195530A CH 195530D A CH195530D A CH 195530DA CH 195530 A CH195530 A CH 195530A
- Authority
- CH
- Switzerland
- Prior art keywords
- preparation
- monoazo dye
- benzoyl
- dye
- amido
- 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
- C09B29/28—Amino naphthols
- C09B29/30—Amino naphtholsulfonic acid
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
Zusatzpatent zum Hauptpatent Nr. 18914 Verfahren zur Darstellung eines Monoazofarbstoffes. Das vorliegende Patent betrifft ein Ver fahren zur Darstellung eines Monoazofarb- stoffes und ist dadurch gekennzeichnet, dass man 4-(N-Benzoyl-N-p-chlorbenzyl)-amido-l- amidobenzol diazotiert und mit N-Benzoyl-r- säure kuppelt.
<I>Beispiel;</I> 33,7 Teile 4-(N-Benzoyl-N-p-chlorbenzyl)- amido-l-amidobenzol werden mit 6,9 Teilen Nitrit und 25 Teilen Salzsäure diazotiert und in Gegenwart von überschüssigem Natrium acetat mit 34,3 Teilen N-Benzoyl-i--säure ge kuppelt. Die Kupplung kann auch in Gegen wart von Natriumbiearbonat oder ähnlich schwach wirkenden Neutralisationsmitteln vor genommen werden. Der isolierte und getrocknete Farbstoff bildet ein rotes Pulver und färbt Wolle und Seide in lebhaften roten Tönen.
Additional patent to main patent No. 18914 Process for the preparation of a monoazo dye. The present patent relates to a method for the preparation of a monoazo dye and is characterized in that 4- (N-benzoyl-N-p-chlorobenzyl) -amido-l-amidobenzene is diazotized and coupled with N-benzoyl-r acid.
<I> Example; </I> 33.7 parts of 4- (N-benzoyl-Np-chlorobenzyl) - amido-l-amidobenzene are diazotized with 6.9 parts of nitrite and 25 parts of hydrochloric acid and in the presence of excess sodium acetate 34.3 parts of N-benzoyl-i - acid coupled. The coupling can also be carried out in the presence of sodium carbonate or similarly weak neutralizing agents. The isolated and dried dye forms a red powder and dyes wool and silk in vivid red tones.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH189141T | 1937-03-18 | ||
CH195530T | 1937-03-18 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH195530A true CH195530A (en) | 1938-01-31 |
Family
ID=25721752
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH195530D CH195530A (en) | 1937-03-18 | 1937-03-18 | Process for the preparation of a monoazo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH195530A (en) |
-
1937
- 1937-03-18 CH CH195530D patent/CH195530A/en unknown
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