GB428468A - Improvements in the manufacture and production of dyestuffs - Google Patents
Improvements in the manufacture and production of dyestuffsInfo
- Publication number
- GB428468A GB428468A GB3160733A GB3160733A GB428468A GB 428468 A GB428468 A GB 428468A GB 3160733 A GB3160733 A GB 3160733A GB 3160733 A GB3160733 A GB 3160733A GB 428468 A GB428468 A GB 428468A
- Authority
- GB
- United Kingdom
- Prior art keywords
- methyl
- ketone
- phenylindolyl
- condensed
- dyestuffs
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
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)
Abstract
Dyestuffs are obtained by condensing by means of phosphorus oxychloride, a b -b <1>-di-indolylketone with a secondary or tertiary aromatic amine or with an indole substituted in the a position by a hydrocarbon radicle. The resulting dyestuffs may be used for colouring cellulose ester lacquers and when sulphonated are suitable for dyeing wool and silk. The secondary and tertiary amines may contain alkyl, alkoxy, aryl, aralkyl and acyl groups. In examples: (1) 4-methyl-3<1>-ethoxydiphenylamine is condensed in toluene with b : b <1>-di(N - methyl - a - phenylindolyl)ketone or b : b <1>-di-(a -methylindolyl)ketone; (2) a keto-chloride compound is first formed from b : b <1>-di-(N-methyl-a -phenylindolyl) ketone, by treatment in tetrachlorethane with phosphorus oxychloride, and 4<1>-3<1>-diethoxy- (or 4-ethoxy) diphenylamine condensed therewith; the resulting basic dyestuff on sulphonation gives a disulphonic acid which dyes wool and silk blue shades; (3) b : b <1>-di-(N-methyl-a -phenylindolyl) ketone is condensed with N-methyl-a -phenylindole and sulphonated to give a trisulphonic acid. b : b <1>-Di-indolylketones may be obtained by reacting two molecular proportions of a or N and a substituted indoles with one molecular proportion of phosgene in a solvent.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB3160733A GB428468A (en) | 1933-11-13 | 1933-11-13 | Improvements in the manufacture and production of dyestuffs |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB3160733A GB428468A (en) | 1933-11-13 | 1933-11-13 | Improvements in the manufacture and production of dyestuffs |
Publications (1)
Publication Number | Publication Date |
---|---|
GB428468A true GB428468A (en) | 1935-05-13 |
Family
ID=10325675
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB3160733A Expired GB428468A (en) | 1933-11-13 | 1933-11-13 | Improvements in the manufacture and production of dyestuffs |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB428468A (en) |
-
1933
- 1933-11-13 GB GB3160733A patent/GB428468A/en not_active Expired
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