GB334240A - Improvements in the manufacture and production of vat dyestuffs of the anthraquinone acridone series - Google Patents
Improvements in the manufacture and production of vat dyestuffs of the anthraquinone acridone seriesInfo
- Publication number
- GB334240A GB334240A GB1669429A GB1669429A GB334240A GB 334240 A GB334240 A GB 334240A GB 1669429 A GB1669429 A GB 1669429A GB 1669429 A GB1669429 A GB 1669429A GB 334240 A GB334240 A GB 334240A
- Authority
- GB
- United Kingdom
- Prior art keywords
- saponified
- acridone
- products
- product
- anthraquinone
- 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
- C09B1/36—Dyes with acylated amino groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
334,240. Johnson, J. Y., (I. G. Farbeninditstrie Akt.-Ges.). May 30, 1929. Anthraquinone acridones. -Vat dyestuffs are prepared by condensing Bz 3: 5-dichloro-4-chloranthraquinone-2 : 1(N)-acridone with amides of aromatic carboxylic or sulphonic acids, and the products saponified if desired. The above acridone-amide condensation products may be obtained more advantageously in some cases by recondensing the saponified products with an aromatic acid chloride. Condensation is preferably carried out in a diluting or suspending medium and in presence of acid-fixing agents; condensing catalysts such as copper or its compounds may also be added. In examples Bz3.5-dichloro-4- chloroanthraquinone-2.1-(N)-acridone (prepared by treating with anthraquinone-2 : 1(N)-acridone suspended in nitrobenzene with sulphuryl chloride in presence of iodinechloride) is condensed (1) with p-toluenesulphonamide and the product saponified by concentrated sulphuric acid at 80‹ C; (2) with benzamide and the product saponified as above; and (3) with either above amide and saponified and the product condensed with 1- chloranthraquinone-2-carboxylic acid chloride. The products dye cotton violet to blue shades.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1669429A GB334240A (en) | 1929-05-30 | 1929-05-30 | Improvements in the manufacture and production of vat dyestuffs of the anthraquinone acridone series |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1669429A GB334240A (en) | 1929-05-30 | 1929-05-30 | Improvements in the manufacture and production of vat dyestuffs of the anthraquinone acridone series |
Publications (1)
Publication Number | Publication Date |
---|---|
GB334240A true GB334240A (en) | 1930-09-01 |
Family
ID=10081928
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1669429A Expired GB334240A (en) | 1929-05-30 | 1929-05-30 | Improvements in the manufacture and production of vat dyestuffs of the anthraquinone acridone series |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB334240A (en) |
-
1929
- 1929-05-30 GB GB1669429A patent/GB334240A/en not_active Expired
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