CH224880A - Process for the production of a vat dye. - Google Patents
Process for the production of a vat dye.Info
- Publication number
- CH224880A CH224880A CH224880DA CH224880A CH 224880 A CH224880 A CH 224880A CH 224880D A CH224880D A CH 224880DA CH 224880 A CH224880 A CH 224880A
- Authority
- CH
- Switzerland
- Prior art keywords
- production
- acid
- dye
- vat dye
- red
- 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
- C09B1/36—Dyes with acylated amino groups
- C09B1/42—Dyes with acylated amino groups the acyl groups being residues of an aromatic carboxylic acid
- C09B1/43—Dicarboxylic acids
-
- 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)
Description
<B>Zusatzpatent</B> zum Hauptpatent Nr. 219414. Verfahren zur Herstellung eines Nüpenfarbstoffes. Es wurde gefunden, dass ein wertvoller Küpenfarbstoff hergestellt werden kann, wenn man 1 Mol der nach dem Verfahren der schweiz. Patentschrift Nr. 208531 erhältlichen Fluoranthendicarbonsäure öder eines ihrer funktionellen Derivate mit 2 Mol 1-Amino- anthrachinon umsetzt.
Der neue Farbstoff stellt ein gelbes Pul ver dar, das sich in konzentrierter Schwefel säure mit roter Farbe löst,'-\bei 4201 unter Zersetzung schmilzt und Baumwolle aus rot brauner Küpe in grünstichiggelben Tönen von sehr guten Echtheitseigenschaften färbt.
Als funktionelle Derivate der Fluoranthen- dicarbonsäure werden zweckmässig ihre Di- halogenide, insbesondere das Dichlorid, das durch Behandeln der freien Dicarbonsäure mit z. B. Thionylchlorid erhältlich ist, ver wendet.
Die Umsetzung erfolgt vorteilhaft durch Erhitzen der Komponenten in Lösungs- oder Verdünnungsmitteln, wie z. B. Di- oder Tri- chlorbenzol, Nitrobenzol, Naphthalin oder Chlornaphthalin.
<I>Beispiel:</I> 14,5 Teile Fluoranthendicarbonsäure wer den durch Erhitzen auf 110-1200 mit 20 Teilen Thionylchlorid in 750 Teilen trocke nem o-Dichlorbenzol in das Säuredichlorid verwandelt.
Nach dem Abdestillieren des un verbrauchten Thionylchlorids lässt man bei 15011 eine heisse Lösung von 22,3 Teilen 1-Ariiinoanthrachinon in 350 Teilen Dichlor- benzol zufliessen. Nach zweistündigem Rühren bei<B>150-1600</B> ist die Farbstoffbildung be endet. Man saugt in der Wärme ab, wäscht mit Dichlorbenzol und Alkohol aus und trocknet.
<B> Additional patent </B> to main patent no. 219414. Process for the production of a pebble dye. It has been found that a valuable vat dye can be produced by using 1 mol of the swiss method. Patent No. 208531 available fluoranthendicarboxylic acid or one of its functional derivatives with 2 moles of 1-aminoanthraquinone.
The new dye is a yellow powder that dissolves in concentrated sulfuric acid with a red color, '- \ at 4201 melts with decomposition and dyes cotton from a red-brown vat in greenish yellow shades with very good fastness properties.
As functional derivatives of the fluoranthene dicarboxylic acid, its dihalides, in particular the dichloride which is obtained by treating the free dicarboxylic acid with z. B. thionyl chloride is available, ver used.
The reaction is advantageously carried out by heating the components in solvents or diluents, such as. B. Di- or trichlorobenzene, nitrobenzene, naphthalene or chloronaphthalene.
<I> Example: </I> 14.5 parts of fluoranthendicarboxylic acid are converted into the acid dichloride by heating to 110-1200 with 20 parts of thionyl chloride in 750 parts of dry o-dichlorobenzene.
After the unused thionyl chloride has been distilled off, a hot solution of 22.3 parts of 1-aryinoanthraquinone in 350 parts of dichlorobenzene is allowed to flow in at 15011. After stirring for two hours at <B> 150-1600 </B>, the dye formation is over. It is suctioned off in the heat, washed with dichlorobenzene and alcohol and dried.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH224880T | 1939-01-19 | ||
CH219414T | 1939-01-19 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH224880A true CH224880A (en) | 1942-12-15 |
Family
ID=25726262
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH224880D CH224880A (en) | 1939-01-19 | 1939-01-19 | Process for the production of a vat dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH224880A (en) |
-
1939
- 1939-01-19 CH CH224880D patent/CH224880A/en unknown
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