GB483402A - Improvements in the manufacture and production of acridone dyestuffs capable of being chromed - Google Patents
Improvements in the manufacture and production of acridone dyestuffs capable of being chromedInfo
- Publication number
- GB483402A GB483402A GB108337A GB108337A GB483402A GB 483402 A GB483402 A GB 483402A GB 108337 A GB108337 A GB 108337A GB 108337 A GB108337 A GB 108337A GB 483402 A GB483402 A GB 483402A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid
- hydroxydiphenylamine
- dinitro
- dicarboxylic acid
- sulpho
- 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
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D219/00—Heterocyclic compounds containing acridine or hydrogenated acridine ring systems
- C07D219/04—Heterocyclic compounds containing acridine or hydrogenated acridine ring systems with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to carbon atoms of the ring system
- C07D219/06—Oxygen atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Abstract
Acridone dyes capable of conversion to complex metal compounds are made by treating with condensing agents diphenylamine-hydroxycarboxylic acids of the general formula <FORM:0483402/IV/1> (in which in the ring I at least one position ortho to the N-atom is unsubstituted, and in which the carboxylic and hydroxy groups in the ring I are in o-position to one another), or their substitution products. The condensing agent may be concentrated sulphuric acid and the ring II may contain one or two nitro groups, or other substituents of acid nature such as halogen atoms. Starting materials specified are those obtained by condensation of 2-alkoxy- or 2-halogen-benzene-1-carboxylic acids (if desired, containing nitro groups in 3- or 5- or 3.5-positions) with o-hydroxybenzene carboxylic acids containing a primary or secondary amino group. In examples: (1) 21.41-dinitro-3-sulpho-6-hydroxydiphenylamine -5.61-dicarboxylic acid is heated with concentrated sulphuric acid (orange shades on wool, brown-red on afterchroming, and red-brown by chrome-printing on cotton); 21- or 41-nitro-3-sulpho-6-hydroxydiphenylamine-5.61 -dicarboxylic acid or 21.41-dinitro-6-hydroxydiphenylamine-5.61 -dicarboxylic acid may also be used; (2) 21.41-dinitro- or 21-or 41 - nitro - 4 - hydroxydiphenylamine-5.61-dicarboxylic acid or their 3-sulpho derivatives are heated with concentrated sulphuric acid to give a product similar to that of example 1. 21.41 - Dinitro - 3 - sulpho - 4(or 6) - hydroxydiphenylamine - 5.61 - dicarboxylic acid is made by condensing 6 (or 2)-hydroxy-3-amino-5 - sulphobenzene - 1 - carboxylic acid with 3.5 - dinitro - 2 - chlorbenzene - 1 - carboxylic acid.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB108337A GB483402A (en) | 1937-01-13 | 1937-01-13 | Improvements in the manufacture and production of acridone dyestuffs capable of being chromed |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB108337A GB483402A (en) | 1937-01-13 | 1937-01-13 | Improvements in the manufacture and production of acridone dyestuffs capable of being chromed |
Publications (1)
Publication Number | Publication Date |
---|---|
GB483402A true GB483402A (en) | 1938-04-20 |
Family
ID=9715868
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB108337A Expired GB483402A (en) | 1937-01-13 | 1937-01-13 | Improvements in the manufacture and production of acridone dyestuffs capable of being chromed |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB483402A (en) |
-
1937
- 1937-01-13 GB GB108337A patent/GB483402A/en not_active Expired
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