GB463045A - Manufacture of derivatives of anthraquinone - Google Patents
Manufacture of derivatives of anthraquinoneInfo
- Publication number
- GB463045A GB463045A GB2568235A GB2568235A GB463045A GB 463045 A GB463045 A GB 463045A GB 2568235 A GB2568235 A GB 2568235A GB 2568235 A GB2568235 A GB 2568235A GB 463045 A GB463045 A GB 463045A
- Authority
- GB
- United Kingdom
- Prior art keywords
- nitrobenzene
- benzoylaminoanthraquinones
- chlorinating
- chloro
- amino
- 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
- C09B1/42—Dyes with acylated amino groups the acyl groups being residues of an aromatic carboxylic acid
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
4.5-, 4.6- and 4.7-Dichloro-1-benzoylaminoanthraquinones, which may be substituted in the benzoyl radical, are made by chlorinating the corresponding 5-, 6-, and 7-chloro-1-benzoylaminoanthraquinones in nitrobenzene or other high-boiling inert solvent in the presence of acetic acid and an acid-binding agent, such as sodium or potassium acetate, or by benzoylating 1-amino-5-, 6-, 7-chloroanthraquinones in nitrobenzene or other high-boiling inert solvent, and then, without isolation of the benzoylamino compound, chlorinating as above. The products are dyestuff intermediates, which yield anthrimides with aminoanthraquinones. In examples, 1-amino-5 (or 6- or 7-)-chloroanthraquinone is benzoylated and chlorinated in nitrobenzene, using acetic acid and sodium acetate during the chlorination. Other solvents specified are trichloro-ethylene, and mono-, di-, and tri-chlorobenzenes. Substituted benzoyl chlorides, such as methyl, chloro, or nitro benzoyl chlorides may be used. Specification 414,529 is referred to.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2568235A GB463045A (en) | 1935-09-16 | 1935-09-16 | Manufacture of derivatives of anthraquinone |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2568235A GB463045A (en) | 1935-09-16 | 1935-09-16 | Manufacture of derivatives of anthraquinone |
Publications (1)
Publication Number | Publication Date |
---|---|
GB463045A true GB463045A (en) | 1937-03-16 |
Family
ID=10231599
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2568235A Expired GB463045A (en) | 1935-09-16 | 1935-09-16 | Manufacture of derivatives of anthraquinone |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB463045A (en) |
-
1935
- 1935-09-16 GB GB2568235A patent/GB463045A/en not_active Expired
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