GB510936A - New process for the manufacture of 1-4-5-8-tetra-aminoanthraquinone - Google Patents
New process for the manufacture of 1-4-5-8-tetra-aminoanthraquinoneInfo
- Publication number
- GB510936A GB510936A GB35180/38A GB3518038A GB510936A GB 510936 A GB510936 A GB 510936A GB 35180/38 A GB35180/38 A GB 35180/38A GB 3518038 A GB3518038 A GB 3518038A GB 510936 A GB510936 A GB 510936A
- Authority
- GB
- United Kingdom
- Prior art keywords
- give
- tetrachloranthraquinone
- tetraminoanthraquinone
- toluenesulphonamide
- dec
- 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
- C09B1/22—Dyes with unsubstituted amino groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
510,936. Aminoanthraquinones. SOC. RHODIACETA. Dec. 2, 1938, No. 35180. Convention date, Dec. 24, 1937. [Class 2 (iii)] 1. 4. 5. 8 - Tetraminoanthraquinone is prepared by reacting 1.4.5.8-tetrachloranthraquinone with p-toluenesulphonamide and hydrolysing the condensation product thus obtained. In an example, anthraquinone is treated with chlorine in sulphuric acid containing a little iodine to give 1.4.5.8.-tetrachloranthraquinone, which is reacted with p-toluenesulphonamide in nitrobenzene in presence of copper powder, copper acetate and potassium carbonate to give a product which is hydrolysed by sulphuric acid to give the sulphate of 1.4.5.8-tetraminoanthraquinone. The free base may be dried in the pure state or mixed with a dispersing agent and dried.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR510936X | 1937-12-24 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB510936A true GB510936A (en) | 1939-08-10 |
Family
ID=8912076
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB35180/38A Expired GB510936A (en) | 1937-12-24 | 1938-12-02 | New process for the manufacture of 1-4-5-8-tetra-aminoanthraquinone |
Country Status (2)
Country | Link |
---|---|
BE (1) | BE510936A (en) |
GB (1) | GB510936A (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2993074A (en) * | 1958-02-10 | 1961-07-18 | Hooker Chemical Corp | Process for the production of phenols by decomposition of aralkyl hydroperoxides |
-
1938
- 1938-12-02 GB GB35180/38A patent/GB510936A/en not_active Expired
-
1952
- 1952-04-24 BE BE510936A patent/BE510936A/en unknown
Also Published As
Publication number | Publication date |
---|---|
BE510936A (en) | 1953-11-06 |
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