CH180278A - Process for the production of a new dye. - Google Patents
Process for the production of a new dye.Info
- Publication number
- CH180278A CH180278A CH180278DA CH180278A CH 180278 A CH180278 A CH 180278A CH 180278D A CH180278D A CH 180278DA CH 180278 A CH180278 A CH 180278A
- Authority
- CH
- Switzerland
- Prior art keywords
- production
- dye
- new dye
- methyl
- dissolves
- 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
- C09B29/06—Monoazo dyes prepared by diazotising and coupling from coupling components containing amino as the only directing group
- C09B29/08—Amino benzenes
-
- 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
- C09B29/0809—Amino benzenes free of acid groups characterised by the amino group substituted amino group
- C09B29/0811—Amino benzenes free of acid groups characterised by the amino group substituted amino group further substituted alkylamino, alkenylamino, alkynylamino, cycloalkylamino aralkylamino or arylamino
- C09B29/0813—Amino benzenes free of acid groups characterised by the amino group substituted amino group further substituted alkylamino, alkenylamino, alkynylamino, cycloalkylamino aralkylamino or arylamino substituted by OH, O-C(=X)-R, O-C(=X)-X-R, O-R (X being O,S,NR; R being hydrocarbonyl)
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Optical Filters (AREA)
- Coloring (AREA)
Description
<B>Zusatzpatent</B> zum Hauptpatent Nr. 178224. Verfahren zur Herstellung eines neuen Farbstoffes. II's wurde gefunden, dass man einen neuen harfistoff erhält, wenn man dia,zotiertes 2- Aiiiino-5-tiitro-phenylmethylsulfon mit 2- Mclhoxy-5-methyl-1. -N-(di-methoxy ä,thyl )- aniinobenzol vereinigt.
Der so erhaltene Farbstoff bildet in trockenem Zustande ein dunkles Pulver, das sich in organischen Lö- snngsinitteln. wie Aceton, Essigester usw., mit leuchtend rotvioletter Farbe löst. Durch ;ee ig-nete Zusätze in feine Verteilung ge- br,icht, färbt er Acetatkunstseide in reinen, violetten Tönen.
<I>Beispiel:</I> ?1,h Teile ?-Amino-5-nitro-phenylmethyl- snlfon werden unter kräftigem Rühren in etwa 3()(l Teilen Schwefelsäure gelöst und darauf durch Zusatz von 8 Teilen Natrium-' nit:rit oder der entsprechenden Menge Nitro- sj#Ischwefelsäure dianotiert. Man rührt, bis eine Probe in Eiswasser klar löslich ist. Nun wird die ganze Mischung in viel Eiswasser gegeben.
Die so erhaltene klare Diazolösung vereinigt man mit einer Auflösung von 25,3 Teilen 2-Methoxy-5-methyl-l-N-(di-methoxy- äthyl)-aminobenzol in der nötigen Menge verdünnter Mineralsäure. Der Farbstoff scheidet sich als dunkles Pulver aus. Nach dem die Kupplung durch Zusatz von Natriumacetat zu Ende geführt wurde, wird filtriert und neutral gewaschen.
<B> Additional patent </B> to main patent no. 178224. Process for the production of a new dye. II's has been found that a new hardener is obtained if one dia, zotierten 2-Aiiiino-5-tiitro-phenylmethylsulfon with 2-methyl-5-methyl-1. -N- (di-methoxy ä, thyl) - aniinobenzene combined.
When dry, the dye thus obtained forms a dark powder which dissolves in organic solvents. like acetone, ethyl acetate, etc., dissolves with a bright red-violet color. Finely distributed through suitable additives, it dyes acetate artificial silk in pure, violet tones.
<I> Example: </I>? 1, h parts of? -Amino-5-nitro-phenylmethyl-snlfon are dissolved in about 3 () (l parts of sulfuric acid) with vigorous stirring and then by adding 8 parts of sodium-nit The mixture is then added to a large amount of ice water and the mixture is poured into a large amount of ice water.
The clear diazo solution thus obtained is combined with a solution of 25.3 parts of 2-methoxy-5-methyl-1-N- (dimethoxy-ethyl) -aminobenzene in the necessary amount of dilute mineral acid. The dye separates out as a dark powder. After the coupling has been completed by adding sodium acetate, the mixture is filtered and washed neutral.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH180278T | 1934-03-24 | ||
CH178224T | 1934-03-24 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH180278A true CH180278A (en) | 1935-10-15 |
Family
ID=25720072
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH180278D CH180278A (en) | 1934-03-24 | 1934-03-24 | Process for the production of a new dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH180278A (en) |
-
1934
- 1934-03-24 CH CH180278D patent/CH180278A/en unknown
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