GB275927A - Improvements in the manufacture and production of benzanthrone derivatives - Google Patents
Improvements in the manufacture and production of benzanthrone derivativesInfo
- Publication number
- GB275927A GB275927A GB6308/27A GB630827A GB275927A GB 275927 A GB275927 A GB 275927A GB 6308/27 A GB6308/27 A GB 6308/27A GB 630827 A GB630827 A GB 630827A GB 275927 A GB275927 A GB 275927A
- Authority
- GB
- United Kingdom
- Prior art keywords
- per cent
- sulphuric acid
- benzanthrone
- derivatives
- cent strength
- 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
- C09B3/00—Dyes with an anthracene nucleus condensed with one or more carbocyclic rings
- C09B3/02—Benzathrones
- C09B3/06—Preparation from starting materials already containing the benzanthrone nucleus
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Indole Compounds (AREA)
Abstract
275,927. I. G. Farbenindustrie Akt.- Ges. Aug. 10, 1926, [Convention date]. Benzanthrene derivatives.-Benzanthrone or its derivatives are. treated with manganese dioxide in presence of sulphuric acid of 65 to 85 per cent strength; the products are not Bz1 : Bz1<1>-dibenzanthronyls, but are soluble in alkali and bisulphite solutions and yield anthraquinone-1-carboxylic acids by action of alkaline oxidizing agents. When 2-substituted benzanthrones are employed, other acid oxidizing agents can be used. Examples are given of the oxidation of benzanthrone and 2- chlorbenzanthrone with manganese dioxide and sulphuric acid of 66 or 77 per cent strength, and of the oxidation of 2- methylbenzanthrone with manganese, dioxide and sulphuric acid of 96 per cent strength; for the latter reaction chromic anhydride or a chromate is also specified as a suitable oxidizing agent. Specifications 251,313 and 278,496 are referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE275927X | 1926-08-10 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB275927A true GB275927A (en) | 1928-06-07 |
Family
ID=6027946
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB6308/27A Expired GB275927A (en) | 1926-08-10 | 1927-03-07 | Improvements in the manufacture and production of benzanthrone derivatives |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB275927A (en) |
-
1927
- 1927-03-07 GB GB6308/27A patent/GB275927A/en not_active Expired
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