CH282628A - Process for the preparation of an indolyl-diphenylmethane dye. - Google Patents
Process for the preparation of an indolyl-diphenylmethane dye.Info
- Publication number
- CH282628A CH282628A CH282628DA CH282628A CH 282628 A CH282628 A CH 282628A CH 282628D A CH282628D A CH 282628DA CH 282628 A CH282628 A CH 282628A
- Authority
- CH
- Switzerland
- Prior art keywords
- indolyl
- dye
- preparation
- condensed
- diphenylmethane dye
- 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
- C09B11/00—Diaryl- or thriarylmethane dyes
- C09B11/04—Diaryl- or thriarylmethane dyes derived from triarylmethanes, i.e. central C-atom is substituted by amino, cyano, alkyl
- C09B11/26—Triarylmethane dyes in which at least one of the aromatic nuclei is heterocyclic
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
Verfahren zur Herstellung eines Indolyl-diphenylmethanfarbstoffes. Gegenstand des vorliegenden Zusatzpaten tes ist ein Verfahren zur Herstellung eines Indolyl-diphenylmethanfarbstoffes, welches dadurch gekennzeichnet ist, dass man 4,4'-Di- chlorbenzophenon-3,3'-disulfosäure mit 1-Me- thyl-2-phenylindol in etwa molekularem Ver hältnis kondensiert und das erhaltene Konden sationsprodukt mit einem Überschuss von o-To- luidin umsetzt.
<I>Beispiel:</I> Man kondensiert 35 Gewichtsteile 4,4'-di- chlorbenzophenon-3,3'-disulfosaures Natrium mit 13,5 Gewichtsteilen 1-Methyl-2-phenyl- indol in 20 Ihiger Schwefelsäure durch 20stün- diges Rühren bei 60 C, saugt das rote Zwi- sehenprodukt ab und verschmilzt mit 100 Ge wichtsteilen o-Toluidin 3 Stunden bei 100 C. Die überschüssige Base entfernt man durch Extraktion mit verdünnter Salzsäure, löst den Farbstoff in verdünnter Sodalösung und salzt mit Kochsalz aus.
Das so erhaltene Produkt stellt ein violett glänzendes Pulver dar, das Wolle aus neutra lem oder saurem Bade in sehr egalen rot stichig blauen Tönen färbt, die sich durch bemerkenswerte Klarheit und eine sehr gute Lichtechtheit auszeichnen.
Process for the preparation of an indolyl-diphenylmethane dye. The subject of the present additional patent is a process for the production of an indolyl-diphenylmethane dye, which is characterized in that 4,4'-dichlorobenzophenone-3,3'-disulfonic acid with 1-methyl-2-phenylindole is approximately molecular Ratio condensed and the condensation product obtained is reacted with an excess of o-toluidine.
<I> Example: </I> 35 parts by weight of 4,4'-dichlorobenzophenone-3,3'-disulfonic acid sodium are condensed with 13.5 parts by weight of 1-methyl-2-phenyl-indole in 20 Ihiger sulfuric acid through 20 hours Stirring at 60 ° C., sucks the red intermediate product off and fuses with 100 parts by weight of o-toluidine for 3 hours at 100 ° C. The excess base is removed by extraction with dilute hydrochloric acid, the dye is dissolved in dilute soda solution and salted with sodium chloride .
The product obtained in this way is a shimmering violet powder that dyes wool from neutral or acidic baths in very even, red, blue tones, which are characterized by remarkable clarity and very good lightfastness.
Claims (1)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE282628X | 1949-04-23 | ||
DE10649X | 1949-06-01 | ||
CH278943T | 1949-06-24 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH282628A true CH282628A (en) | 1952-04-30 |
Family
ID=27178133
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH282628D CH282628A (en) | 1949-04-23 | 1949-06-24 | Process for the preparation of an indolyl-diphenylmethane dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH282628A (en) |
-
1949
- 1949-06-24 CH CH282628D patent/CH282628A/en unknown
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