GB337047A - Process for the manufacture of aminohydroxyanthraquinones and substitution products thereof - Google Patents
Process for the manufacture of aminohydroxyanthraquinones and substitution products thereofInfo
- Publication number
- GB337047A GB337047A GB2305029A GB2305029A GB337047A GB 337047 A GB337047 A GB 337047A GB 2305029 A GB2305029 A GB 2305029A GB 2305029 A GB2305029 A GB 2305029A GB 337047 A GB337047 A GB 337047A
- Authority
- GB
- United Kingdom
- Prior art keywords
- amino
- hydroxy
- phthalic anhydride
- urea
- give
- 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
- C09B1/18—Preparation by synthesis of the nucleus
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
337,047. Carpmael, A., (I. G. F'arbenindustrie Akt.-Ges.). July 26, 1929. Aminohydroxyanthraquinones and substitution products thereof are obtained by condensing an acyl- or aroyl-aminophenol, homologue or substitution product thereof with phthalic anhydride, or a substitution product thereof, in presence of an agent such as aluminium chloride, saponifying and ring-closing when necessary in the customary manner. According to examples, (1) 2: 3- aminohydroxyanthraquinone is obtained by condensing 2 : 2<1> - dimethoxydiphenyl urea and phthalic anhydride in presence of aluminium and sodium chlorides, followed by ring-closure of the benzoyl benzoic acid formed intermediately and saponification; the corresponding 1: 2-compound is also formed; (2) 1-amino-4-hydroxyanthraquinone is obtained in a similar manner from 1- benzoylamino-4-phenol with the intermediate formation of a benzoyl benzoic acid derivative; (3) o-dimethoxydiphenyl urea is condensed with 3-chlorophthalic anhydride to give a 3'-amino-4'- hydroxy (or methoxy)-6-chlorobenzoyl-2-benzoic acid, and, then the 2-amino-3-hydroxy-5-chloroanthraquinone; (4) 1-amino-3-chloro-6-methoxybenzene and phthalic anhydride give the 1- hydroxy-2-amino-4-chloroanthraquinone; (5) the the urea from 1-amino-3-methyl-6-methoxybenzene and phthalic anhydride is similarly condensed to give the 1 - hydroxy - 4 - methyl-2-aminoanthraquinone.
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEI38542D DE538457C (en) | 1929-06-29 | 1929-06-29 | Process for the preparation of aminooxyanthraquinones and their substitution products |
GB2305029A GB337047A (en) | 1929-07-26 | 1929-07-26 | Process for the manufacture of aminohydroxyanthraquinones and substitution products thereof |
US464419A US1922480A (en) | 1929-06-29 | 1930-06-27 | Manufacture of amino-hydroxyanthraquinones |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2305029A GB337047A (en) | 1929-07-26 | 1929-07-26 | Process for the manufacture of aminohydroxyanthraquinones and substitution products thereof |
Publications (1)
Publication Number | Publication Date |
---|---|
GB337047A true GB337047A (en) | 1930-10-27 |
Family
ID=10189288
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2305029A Expired GB337047A (en) | 1929-06-29 | 1929-07-26 | Process for the manufacture of aminohydroxyanthraquinones and substitution products thereof |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB337047A (en) |
-
1929
- 1929-07-26 GB GB2305029A patent/GB337047A/en not_active Expired
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