GB311283A - - Google Patents
Info
- Publication number
- GB311283A GB311283A GB14258/29A GB1425829A GB311283A GB 311283 A GB311283 A GB 311283A GB 14258/29 A GB14258/29 A GB 14258/29A GB 1425829 A GB1425829 A GB 1425829A GB 311283 A GB311283 A GB 311283A
- Authority
- GB
- United Kingdom
- Prior art keywords
- aminoanthraquinone
- benzoylamino
- product
- products
- 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
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10K—PURIFYING OR MODIFYING THE CHEMICAL COMPOSITION OF COMBUSTIBLE GASES CONTAINING CARBON MONOXIDE
- C10K1/00—Purifying combustible gases containing carbon monoxide
- C10K1/04—Purifying combustible gases containing carbon monoxide by cooling to condense non-gaseous materials
- C10K1/06—Purifying combustible gases containing carbon monoxide by cooling to condense non-gaseous materials combined with spraying with water
-
- 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
- C09B1/34—Dyes with amino groups substituted by hydrocarbon radicals substituted by aryl groups sulfonated
-
- G—PHYSICS
- G11—INFORMATION STORAGE
- G11B—INFORMATION STORAGE BASED ON RELATIVE MOVEMENT BETWEEN RECORD CARRIER AND TRANSDUCER
- G11B7/00—Recording or reproducing by optical means, e.g. recording using a thermal beam of optical radiation by modifying optical properties or the physical structure, reproducing using an optical beam at lower power by sensing optical properties; Record carriers therefor
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Combustion & Propulsion (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
311,283. I. G. Farbenindustrie Akt.- Ges. May 8, 1928, [Convention date]. Anthraquinone acridones.- Dianthraquinonylamines of the anthraquinoneacridone series are obtained by causing an aminoanthraquinone or a derivative or substitution product thereof to act on a polyhalogen anthraquinone-N-1 : 2-acridone, containing, in addition to halogen in the phenyl residue a halogen atom in the 4-position of the anthraquinone nucleus, in a high-boiling solvent in the presence of an acid-fixing agent and, as catalyst, copper or a salt thereof. The products are themselves vat dyes, and can be used as intermediates for the production or other vat dyes. In examples, trichloranthraquinacridone is heated in the presence of naphthalene, sodium acetate and cupric chloride with 1-benzoylamino- 4- or 5- aminoanthraquinone, and with 1-aminoanthraquinone; the products dye cotton from an alkaline hydrosulphite vat in grey shades. The product from 1-benzoylamino-5-aminoanthraquinone is identical with the condensation product from Bz-dichlor-4-aminoanthraquinoneacridone (made in accordance with Specification 17764/14, by the use of 3 : 5-dichlor-2-anthranilic acid) and 1-benzoylamino-5-chloranthraquinone Specification 305,082 also is referred to. The Specification as open to inspection under Sect. 91 (3) (a) is not limited to the use of copper or salts thereof as catalysts, and includes an additional example in which a. product dyeing cotton in corinth shades is obtained from trichloranthraquinoneacridone and 1-amino-4-methoxyanthroquinone. It also states that vat dyes of different shade and apparently of carbazole structure may be obtained by treating the products with condensing agents. This subject-matter does not appear in the Specification as accepted.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE311283T | 1928-05-08 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB311283A true GB311283A (en) | 1930-08-07 |
Family
ID=31894605
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB14258/29A Expired GB311283A (en) | 1928-05-08 | 1929-05-07 |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB311283A (en) |
-
1929
- 1929-05-07 GB GB14258/29A patent/GB311283A/en not_active Expired
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