GB1074829A - Anthraquinone dyestuffs - Google Patents
Anthraquinone dyestuffsInfo
- Publication number
- GB1074829A GB1074829A GB1963265A GB1963265A GB1074829A GB 1074829 A GB1074829 A GB 1074829A GB 1963265 A GB1963265 A GB 1963265A GB 1963265 A GB1963265 A GB 1963265A GB 1074829 A GB1074829 A GB 1074829A
- Authority
- GB
- United Kingdom
- Prior art keywords
- ester
- carboxylic acid
- acid
- anthraquinone
- copper
- 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
- C09B1/00—Dyes with anthracene nucleus not condensed with any other ring
- C09B1/16—Amino-anthraquinones
- C09B1/20—Preparation from starting materials already containing the anthracene nucleus
- C09B1/26—Dyes with amino groups substituted by hydrocarbon radicals
- C09B1/32—Dyes with amino groups substituted by hydrocarbon radicals substituted by aryl groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Coloring (AREA)
Abstract
The invention comprises dyestuffs of the general formula <FORM:1074829/C4-C5/1> wherein R1 and R2 are hydrogen or a group <FORM:1074829/C4-C5/2> wherein one of X1 and X2 is hydrogen and the other a carboxylic acid group. They are prepared by heating the corresponding halogeno-anthraquinone and amino substituted carboxylic acid, or an ester thereof, or by heating the corresponding amino anthraquinone and halogeno benzene carboxylic acid or ester in a solvent e.g. benzyl alcohol or nitrobenzene and in the presence of an acid binding agent e.g. sodium carbonate or potassium acetate, a copper catalyst e.g. copper bronze or copper acetate, and potassium iodide. Ester groups are subsequently hydrolysed by caustic alkali. In an alternative method of preparation, leucoquinzarin is reacted with m-aminobenzoic acid in a solvent e.g. butanol in presence of boric acid or an ester thereof.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1963265A GB1074829A (en) | 1964-06-08 | 1964-06-08 | Anthraquinone dyestuffs |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1963265A GB1074829A (en) | 1964-06-08 | 1964-06-08 | Anthraquinone dyestuffs |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1074829A true GB1074829A (en) | 1967-07-05 |
Family
ID=10132605
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1963265A Expired GB1074829A (en) | 1964-06-08 | 1964-06-08 | Anthraquinone dyestuffs |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB1074829A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1930377A3 (en) * | 2006-12-07 | 2009-07-15 | Lanxess Deutschland GmbH | Method for producing substituted aminoanthraquinones |
-
1964
- 1964-06-08 GB GB1963265A patent/GB1074829A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1930377A3 (en) * | 2006-12-07 | 2009-07-15 | Lanxess Deutschland GmbH | Method for producing substituted aminoanthraquinones |
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