CH238268A - Process for the preparation of a new dye of the anthraquinone series. - Google Patents
Process for the preparation of a new dye of the anthraquinone series.Info
- Publication number
- CH238268A CH238268A CH238268DA CH238268A CH 238268 A CH238268 A CH 238268A CH 238268D A CH238268D A CH 238268DA CH 238268 A CH238268 A CH 238268A
- Authority
- CH
- Switzerland
- Prior art keywords
- dye
- preparation
- anthraquinone series
- parts
- new dye
- Prior art date
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
- C09B1/34—Dyes with amino groups substituted by hydrocarbon radicals substituted by aryl groups sulfonated
- C09B1/343—Dyes with amino groups substituted by hydrocarbon radicals substituted by aryl groups sulfonated only sulfonated in the anthracene nucleus
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
<B>Brevet</B> additionnel subordonné au brevet principal no 236390. Procédé de préparation d'un nouveau colorant de la série anthraquinonique. Le présent brevet a pour objet un pro cédé de préparation -d'un nouveau colorant de la série anthraquinonique, selon lequel on condense l'acide 1-amino-2,4-dibromauthra- quinone-6-,sulfonique avec la 3-(méthylacétyl- amino)
-aniline et traite le colorant monosul- foné ainsi obtenu à chaud avec un sulfite.
Le colorant ainsi préparé correspond à la formule suivante:
EMI0001.0016
et teint les fibres animales en bleu verdâtre, ayant -de bonnes propriétés.
Exemple: On chauffe ensemble pendant 20 heures à 80 : 10 parties de 1-amino-2,4-,dibrom- anthraquinone - 6 - sulfonate -de potassium, 7,3 parties de 3-(méthylacétylamino)-aniline, 4,8 parties de bicarbonate ,de sodium, 0,2 par tie de poudre de cuivre, 50 parties d'eau et 15 parties. d'alcool.
On sépare le colorant monosulfoné formé et on le traite au sulfite pour introduire, à la place -du brome qui s'y trouve, un groupe sulfonique en position 2. Cette opération se fait par exemple ainsi: On chauffe pendant quelques heures, en vase ouvert ou fermé, entre 100 et 140 : 10 par ties .du colorant monosulfoné, 20 parties de phénol, 20 parties d'une solution de sulfite de sodium 35-40% en poids.
Quand la ré action est terminée,' on chasse le phénol à la vapeur d'eau, on filtre la solution bleue à chaud, pour éliminer les produits insolubles éventuels, on précipite le colorant dis ulfoné par adjonction de sel et filtre le colorant qui s'est séparé. . Le colorant ainsi obtenu correspond à la formule
EMI0002.0002
et teint les fibres animales en bleu verdâtre. ayant de bonnes propriétés.
Additional <B> Patent </B> subject to main patent No. 236390. Process for preparing a new dye of the anthraquinone series. The present patent relates to a process for the preparation of a new dye of the anthraquinone series, according to which 1-amino-2,4-dibromauthraquinone-6-, sulfonic acid is condensed with 3- ( methylacetylamino)
-aniline and treats the monosulfonate dye thus obtained hot with a sulfite.
The dye thus prepared corresponds to the following formula:
EMI0001.0016
and dyes the animal fibers greenish blue, having good properties.
Example: Heated together for 20 hours at 80: 10 parts of 1-amino-2,4-, dibrom- anthraquinone - 6 - potassium sulfonate, 7.3 parts of 3- (methylacetylamino) -aniline, 4.8 parts of bicarbonate, sodium, 0.2 parts of copper powder, 50 parts of water and 15 parts. alcohol.
The monosulfonated dye formed is separated and treated with sulfite to introduce, in place of the bromine which is therein, a sulfonic group in position 2. This operation is done for example as follows: It is heated for a few hours, in a vase open or closed, between 100 and 140: 10 parts of monosulfonated dye, 20 parts of phenol, 20 parts of sodium sulfite solution 35-40% by weight.
When the reaction is complete, the phenol is driven off with water vapor, the blue solution is filtered hot, to remove any insoluble products, the dissolved dye is precipitated by adding salt and the dye which s 'is separated. . The dye thus obtained corresponds to the formula
EMI0002.0002
and dyes the animal fibers a greenish blue. having good properties.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH238268T | 1943-07-16 | ||
CH236390T | 1943-07-16 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH238268A true CH238268A (en) | 1945-06-30 |
Family
ID=25728100
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH238268D CH238268A (en) | 1943-07-16 | 1943-07-16 | Process for the preparation of a new dye of the anthraquinone series. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH238268A (en) |
-
1943
- 1943-07-16 CH CH238268D patent/CH238268A/en unknown
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