GB300432A - Improvements in the manufacture and production of vat dyestuffs - Google Patents
Improvements in the manufacture and production of vat dyestuffsInfo
- Publication number
- GB300432A GB300432A GB318728A GB318728A GB300432A GB 300432 A GB300432 A GB 300432A GB 318728 A GB318728 A GB 318728A GB 318728 A GB318728 A GB 318728A GB 300432 A GB300432 A GB 300432A
- Authority
- GB
- United Kingdom
- Prior art keywords
- dibenzanthronyl
- aminoanthraquinone
- molecular parts
- dibenzanthronyls
- tetrabrom
- 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
- C09B3/12—Dibenzanthronyls
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
300,432. Johnsonn, J. Y., (I. G. Farbenindustrie Akt.-Ges.). Feb. 1, 1928. Anthraquinone vat dyes are obtained by condensing a tetrahalogen-2 : 2<1>-dibenzanthronyl with an aminoanthraquinone, preferably in presence of acid-fixing agents and of catalysts such as copper or its salts. The condensation appears to proceed further than to anthraquinonylamino-2 2<1>- dibenzanthronyls. In examples, tetrabrom-2 2<1>- dibenzanthronyl is condensed with cupric oxide and calcined soda as assistants, and without any diluent, with two molecular parts of a- or #- aminoanthraquinone, 2-amino-3-chloranthraquinone, or a- or #-aminoalizarin, or, in nitrobenzene as solvent, with two molecular parts of aaminoanthraq uinone, 1-amino-4-methoxyanthraquinone, or 1 : 6-diaminoanthraquinone; dibrom- 6 : 6<1>-dichlordibenzanthronyl is condensed with two molecular parts of alpha-aminoanthraquinone, in nitrobenzene solution, with copper oxide and calcined soda as assistants. Dibenzanthronyls. - Tetrabrom-2: 2'dibenzanthronyl is prepared by brominating 2 : 2<1>-di benzanthronyl in chlorsulphonic acid, or with excess of liquid bromine. Dibrom-6 : 6<1>-dichlor- 2 : 2<1>-dibenzanthronyl is prepared by introducing 6 : 6<1>-dichlor-2 : 2<1>-dibenzanthronyl into excess of bromine.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB318728A GB300432A (en) | 1928-02-01 | 1928-02-01 | Improvements in the manufacture and production of vat dyestuffs |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB318728A GB300432A (en) | 1928-02-01 | 1928-02-01 | Improvements in the manufacture and production of vat dyestuffs |
Publications (1)
Publication Number | Publication Date |
---|---|
GB300432A true GB300432A (en) | 1928-11-15 |
Family
ID=9753559
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB318728A Expired GB300432A (en) | 1928-02-01 | 1928-02-01 | Improvements in the manufacture and production of vat dyestuffs |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB300432A (en) |
-
1928
- 1928-02-01 GB GB318728A patent/GB300432A/en not_active Expired
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