GB191321133A - Improvements in the Manufacture of Colouring Matters of the Anthracene Series. - Google Patents
Improvements in the Manufacture of Colouring Matters of the Anthracene Series.Info
- Publication number
- GB191321133A GB191321133A GB191321133DA GB191321133A GB 191321133 A GB191321133 A GB 191321133A GB 191321133D A GB191321133D A GB 191321133DA GB 191321133 A GB191321133 A GB 191321133A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid
- carboxylic acid
- carboxylic
- treating
- dichlorfluorenone
- 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
- C09B1/26—Dyes with amino groups substituted by hydrocarbon radicals
- C09B1/32—Dyes with amino groups substituted by hydrocarbon radicals substituted by aryl groups
- C09B1/325—Dyes with no other substituents than the amino groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
21,133. Johnson, J. Y., [Badische Anilin & Soda Fabrik]. Sept. 18. Samples furnished. Anthracene, dyes derived from.-Vat dyes are obtained by condensing 1-aminoanthraquinone, or derivatives thereof, with halogenfluorenone carboxylic acids; the carboxylic group splits off during the condensation; the products are identical with those described in Specification 7632/10. According to examples, 1-aminoanthraquinone is condensed with dichlorfluorenone- 4-carboxylic acid, 2: 7-dibromfluorenone-4-carboxylic acid, and bromfluorenone carboxylic acid. Dichlorfluorenone-4-carboxylic acid is obtained by treating fluorenone-4-carboxylic acid with fuming sulphuric acid, and treating the resulting disulphonic acid with sodium chlorate and hydrochloric acid. 2:7-Dibromfluorenone-4-carboxylic acid is obtain by treating diazotized bromanthranilic acid with an ammoniacal solution of cuprous ammonium sulphite, and heating the resulting 4:4<1>- dibromdiphenyl-2 : 2<1>-dicarboxylic acid with concentrated sulphuric acid. Monobromfluorenone carboxylic acid is obtained by heating 4-bromdiphenyl-2: 2<1>-dicarboxylic acid with concentrated sulphuric acid.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB191321133T | 1913-09-18 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB191321133A true GB191321133A (en) | 1914-07-23 |
Family
ID=32646370
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB191321133D Expired GB191321133A (en) | 1913-09-18 | 1913-09-18 | Improvements in the Manufacture of Colouring Matters of the Anthracene Series. |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB191321133A (en) |
-
1913
- 1913-09-18 GB GB191321133D patent/GB191321133A/en not_active Expired
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