CH228830A - Process for the preparation of a dye of the stilbene series. - Google Patents
Process for the preparation of a dye of the stilbene series.Info
- Publication number
- CH228830A CH228830A CH228830DA CH228830A CH 228830 A CH228830 A CH 228830A CH 228830D A CH228830D A CH 228830DA CH 228830 A CH228830 A CH 228830A
- Authority
- CH
- Switzerland
- Prior art keywords
- dye
- stilbene
- preparation
- parts
- stilbene series
- 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
- C09B56/00—Azo dyes containing other chromophoric systems
- C09B56/04—Stilbene-azo dyes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
Zusatzpatent zum Hauptpatent Nr. 21723e. Verfahren zur Herstellung eines Farbstoffes der Stilbenreihe. Es wurde gedunden, dass ein neuer Farb stoff dex Stil!benrelhe 'hergestellt werdren kann, wenn man dem Farbstoff, der durch vorsichtige Reduktion von 4,4'-Dinitrostilben, 2,2'-.düulfon;
siäure unter Verknüpfung zweier Moleküle erhalten wird, mit 1 Mol des Farb stoffes dler Formel
EMI0001.0025
kondensiert. Der neue Farbstoff stellt .getrocknet ein braunes Pulver dar, das sieh in konzentrIer- ter Sohwefelsäure mit blauer,
in Waeser mit brauno,rani-er Farbe löst und Baumwolle bei Gegenwart von Kupfersalzen in echten, brau nen Tönen färbt.
Dar dem Verfahren als Ausgangsstoff dienende -Stilben.farbstoff ist als ein Gemisch der Produkte der Formeln
EMI0001.0049
aufzufassen. Die Kon@dlensation kann beispielsweise durch Erhitzen der Komponenten in alka lischem, vorzugsweise ätzalkalisehem Me dium, offen oder unter Druck, durchgeführt werden.
Beispiel: 18 Teile des Farbstoffes, der erhalten wird, wenn man 45 Teile 4,4'-,diuitrostilben- 2,2'.disulfonsaures Natrium mit 7 Teilen Traubenzucker und 60 Teilen 30 % iger Na tronlauge, in etwa 400 Teilen Wasser ge löst, bei 70 bis 80 reduziert und den Farb stoff in bekannter Weise durch Neutralisie ren und Zugabe von Natriumachlorid abschei det,
und 6 Teile ödes Natriumsalzes: .der 4-. Amino - 4'-oxy - ä'- methylazobenzol - 5'- car- bonsäure werden in 200 Teilen Wasser und 18 Teilen f0 % iger Natriumhydroxydlösung gelöst und 12 Stunden rückfliessend gekocht. Nach dem Erkalten wird Jer ausgefallene Farbstoff <RTI
ID="0002.0038"> abfiltriert; sollte er noch etwas un- veränderten Monoazofarbstoff enthalten, so wird er unter Zusatz von etwas Natrium hydroxyd in heissem Wasser gelöst und durch Zusatz von ca. 5 % Chlornatrium wieder aus gefällt.
Additional patent to main patent No. 21723e. Process for the preparation of a dye of the stilbene series. It was invented that a new dye dex Stil Benrelhe 'could be produced if the dye, which was obtained by careful reduction of 4,4'-dinitrostilbene, 2,2' -. Düulfon;
Acid is obtained by linking two molecules, with 1 mole of the dye of the formula
EMI0001.0025
condensed. When dried, the new dye is a brown powder that looks in concentrated sulfuric acid with blue,
Dissolves in water with brown, rani-er color and dyes cotton in the presence of copper salts in real, brown tones.
The -stilbene dye, which serves as the starting material for the process, is available as a mixture of the products of the formulas
EMI0001.0049
understand. The condensation can be carried out, for example, by heating the components in an alkaline, preferably caustic alkali, medium, openly or under pressure.
Example: 18 parts of the dye obtained when 45 parts of 4,4 ', diuitrostilbene 2,2'.disulfonic acid sodium with 7 parts of grape sugar and 60 parts of 30% sodium hydroxide solution are dissolved in about 400 parts of water , reduced at 70 to 80 and the dye separated in the known manner by neutralizing and adding sodium chloride,
and 6 parts of the desolate sodium salt: the 4-. Amino-4'-oxy-ä'-methylazobenzene-5'-carboxylic acid are dissolved in 200 parts of water and 18 parts of f0% sodium hydroxide solution and refluxed for 12 hours. After cooling, the precipitated dye becomes <RTI
ID = "0002.0038"> filtered off; should it still contain some unchanged monoazo dye, it is dissolved in hot water with the addition of a little sodium hydroxide and precipitated out again by adding about 5% sodium chloride.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH228830T | 1940-07-06 | ||
CH217235T | 1941-10-15 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH228830A true CH228830A (en) | 1943-09-15 |
Family
ID=25725977
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH228830D CH228830A (en) | 1940-07-06 | 1940-07-06 | Process for the preparation of a dye of the stilbene series. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH228830A (en) |
-
1940
- 1940-07-06 CH CH228830D patent/CH228830A/en unknown
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