CH198316A - Process for the preparation of a monoazo dye. - Google Patents
Process for the preparation of a monoazo dye.Info
- Publication number
- CH198316A CH198316A CH198316DA CH198316A CH 198316 A CH198316 A CH 198316A CH 198316D A CH198316D A CH 198316DA CH 198316 A CH198316 A CH 198316A
- Authority
- CH
- Switzerland
- Prior art keywords
- preparation
- monoazo dye
- dye
- amido
- acid
- 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
<B>Zusatzpatent</B> zum Hauptpatent Nr. 189141. Verfahren zur Darstellung eines Ilonoazofarbstoffes. Das vorliegende Patent betrifft ein Ver fahren zur Darstellung eines Monoazofarb- stoffes und ist dadurch gekennzeichnet, dass man 4-(N-o-Chlorbenzoyl-N-benzyl)-amido-l- amidobenzol diazotiert und mit N-Benzoyl-r- säure kuppelt.
<I>Beispiel:</I> 33,7 Teile 4-(N-o-Chlorbenzoyl-N-benzyl)- 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-r-säure ge kuppelt. Die Kupplung kann auch in Gegen wart von Nätriumbicarbonat oder ähnlich schwachwirkenden Neutralisätionsmitteln vor genommen werden,. Der isolierte und getrocknete Farbstoff stellt ein rotes Pulver dar und färbt Wolle und Seide in lebhaften roten Tönen.
<B> Additional patent </B> to main patent no. 189141. Process for the preparation of an ilonoazo dye. The present patent relates to a process for the preparation of a monoazo dye and is characterized in that 4- (N-o-chlorobenzoyl-N-benzyl) -amido-l-amidobenzene is diazotized and coupled with N-benzoyl-r-acid.
<I> Example: </I> 33.7 parts of 4- (No-chlorobenzoyl-N-benzyl) - 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 with 34.3 parts of N-benzoyl-r-acid coupled. The coupling can also be made in the presence of sodium bicarbonate or similar weakly acting neutralizing agents. The isolated and dried dye is 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 |
---|---|---|---|
CH198316T | 1937-03-18 | ||
CH189141T | 1937-03-18 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH198316A true CH198316A (en) | 1938-06-15 |
Family
ID=25721754
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH198316D CH198316A (en) | 1937-03-18 | 1937-03-18 | Process for the preparation of a monoazo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH198316A (en) |
-
1937
- 1937-03-18 CH CH198316D patent/CH198316A/en unknown
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