GB650928A - Process for the manufacture of sulphonated carbazole derivatives of the anthraquinone series - Google Patents
Process for the manufacture of sulphonated carbazole derivatives of the anthraquinone seriesInfo
- Publication number
- GB650928A GB650928A GB32976/48A GB3297648A GB650928A GB 650928 A GB650928 A GB 650928A GB 32976/48 A GB32976/48 A GB 32976/48A GB 3297648 A GB3297648 A GB 3297648A GB 650928 A GB650928 A GB 650928A
- Authority
- GB
- United Kingdom
- Prior art keywords
- benzoylamino
- anthraquinone
- acylamino
- sulphonated
- sulphonating agents
- 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
- C09B5/00—Dyes with an anthracene nucleus condensed with one or more heterocyclic rings with or without carbocyclic rings
- C09B5/24—Dyes with an anthracene nucleus condensed with one or more heterocyclic rings with or without carbocyclic rings the heterocyclic rings being only condensed with an anthraquinone nucleus in 1-2 or 2-3 position
- C09B5/26—Carbazoles of the anthracene series
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Indole Compounds (AREA)
Abstract
Sulphonated carbazoles are made by treating with sulphonating agents at 0-60 DEG C. anthraquinone compounds of the formula <FORM:0650928/IV (c)/1> where X is hydrogen, halogen, alkyl, or alkoxy, and Y is hydrogen, alkyl, halogen, or acylamino. The products dye wool, leather, super-polyamides, and natural silk brown-yellow to brown shades. Sulphonating agents are concentrated sulphuric acid, the monohydrate, oleum, and chlorsulphonic acid, or mixtures thereof. The 1-acylamino groups may be acetylamino, chloracetylamino, propionylamino, phenylacetylamino, hexahydrobenzoylamino, benzoylamino, halogenbenzoylamino, nitrobenzoylamino, amino- or methoxy-benzoylamino, and phthaloylamino. The starting materials are prepared by condensing a 1.5-aminohalogenanthraquinone with an aminodiphenyl followed by acylation, or from a 1-acylamino - 5 - halogenanthraquinone and an aminodiphenyl, followed by acylation, if necessary. Examples describe the treatment with sulphonating agents of 1-benzoylamino-5-(41-phenylamilino)-anthraquinone and of 1-benzoylamino - 5 - benzoylbenzidino - anthraquinone. A further list of starting materials variously substituted as indicated is also given.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH650928X | 1947-12-29 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB650928A true GB650928A (en) | 1951-03-07 |
Family
ID=4526104
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB32976/48A Expired GB650928A (en) | 1947-12-29 | 1948-12-21 | Process for the manufacture of sulphonated carbazole derivatives of the anthraquinone series |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB650928A (en) |
-
1948
- 1948-12-21 GB GB32976/48A patent/GB650928A/en not_active Expired
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