GB470529A - The manufacture of vat dyestuffs - Google Patents
The manufacture of vat dyestuffsInfo
- Publication number
- GB470529A GB470529A GB19895/36A GB1989536A GB470529A GB 470529 A GB470529 A GB 470529A GB 19895/36 A GB19895/36 A GB 19895/36A GB 1989536 A GB1989536 A GB 1989536A GB 470529 A GB470529 A GB 470529A
- Authority
- GB
- United Kingdom
- Prior art keywords
- product
- aminoanthraquinone
- residue
- treated
- 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
- C09B5/00—Dyes with an anthracene nucleus condensed with one or more heterocyclic rings with or without carbocyclic rings
- C09B5/24—Dyes with an anthracene nucleus condensed with one or more heterocyclic rings with or without carbocyclic rings the heterocyclic rings being only condensed with an anthraquinone nucleus in 1-2 or 2-3 position
- C09B5/34—Anthraquinone acridones or thioxanthrones
- C09B5/40—Condensation products of benzanthronyl-amino-anthraquinones
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Vat dyes are made by treating with acylating agents the alkaline condensation products of such 1-(Bz.1-benzanthronyl-amino)-4- or -5-or -8- aminoanthraquinones as contain in the 5- or 6- or 7- or 8- position of the benzanthrone nucleus the residue of a further amine of the anthraquinone series. In examples, (1) the condensation product of the formula <FORM:0470529/IV/1> (obtained by treating with caustic alkali the product obtainable by consecutive condensation of Bz.1-6-dibromobenzanthrone with one mol. of 1-amino-5-benzoylaminoanthraquinone and 1 mol. of 1-aminoanthraquinone, the benzoyl group being split off by the caustic alkali) or the corresponding body containing in the 6-position of the benzanthrone nucleus the residue of 2-aminoanthraquinone or of 6-chloro-6-aminoanthraquinone is treated with benzoyl chloride or a halogenated derivative thereof or with anthraquinone-2-carboxylic acid chloride; (2) the product of the above formula but containing the NH2 group in the 4- or 8- position of the anthraquinone residue is treated with benzoyl chloride; (3) and (4) the product of the above formula is treated respectively with acetic anhydride, and with 1-nitroanthraquinone-2-carboxylic acid chloride. Specifications 337,741 and 339,396, [both in Class 2 (iii)], are referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE470529X | 1935-07-17 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB470529A true GB470529A (en) | 1937-08-17 |
Family
ID=6541138
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB19895/36A Expired GB470529A (en) | 1935-07-17 | 1936-07-17 | The manufacture of vat dyestuffs |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB470529A (en) |
-
1936
- 1936-07-17 GB GB19895/36A patent/GB470529A/en not_active Expired
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