CH224882A - Process for the production of a vat dye. - Google Patents
Process for the production of a vat dye.Info
- Publication number
- CH224882A CH224882A CH224882DA CH224882A CH 224882 A CH224882 A CH 224882A CH 224882D A CH224882D A CH 224882DA CH 224882 A CH224882 A CH 224882A
- Authority
- CH
- Switzerland
- Prior art keywords
- production
- dye
- acid
- vat dye
- fluoranthendicarboxylic
- 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
- C09B5/00—Dyes with an anthracene nucleus condensed with one or more heterocyclic rings with or without carbocyclic rings
- C09B5/02—Dyes with an anthracene nucleus condensed with one or more heterocyclic rings with or without carbocyclic rings the heterocyclic ring being only condensed in peri position
- C09B5/16—Benz-diazabenzanthrones, e.g. anthrapyrimidones
-
- 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 Nüpenfarbstoifes. Es wurde gefunden, dass ein wertvoller Küpenfarbstoff hergestellt werden kann, wenn man 1 Mol der nach dem Verfahren der schweiz. Patentschrift Nr.<B>208531</B> erhält lichen Fluoranthendicarbonsäure oder eines ihrer funktionellen Derivate mit 2 Mol 4-Amino-1,9-anthrapyrimidin umsetzt.
Der neue Farbstoff stellt ein gelbes Pul ver dar, das sieh in konzentrierter Schwefel säure mit roter Farbe löst, sich bei 400 zer setzt und Baumwolle aus brauner Küpe in grünstiohiggelben Tönen färbt.
Als funktionelle Derivate der Fluor- anthendicarbonsäure werden zweckmässig ihre Dihalagenide, insbesondere das Di- chlorid, .das durch Behandeln der freien Di- carb.onsäure mit z. B. Thionylchlorid erhält lich ist, verwendet.
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 110-120' mit 20 Teilen Thionylchlorid in 750 Teilen trockenem o-Dichlorbenzol in das Säure- dichlorid verwandelt.
Nach dem Ab-destillie- ren des unverbrauchten Thionylchlorids lässt man bei 150 eine heisse Lösung von 24,7 Tei len 4-Amino-1,9-anthrapyrimidin in<B>350</B> Tei len Dichlorbenzol zufliessen. Nach zweistün digem Rühren bei 150-160' ist die Farb- stoffbildung beendet. 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 pomaceous dye. It has been found that a valuable vat dye can be produced if 1 mole of the can be produced using the Swiss method. Patent No. 208531 obtained by converting fluoranthendicarboxylic acid or one of its functional derivatives with 2 moles of 4-amino-1,9-anthrapyrimidine.
The new dye is a yellow powder that dissolves in concentrated sulfuric acid with a red color, decomposes at 400 and dyes cotton from a brown vat in greenish-yellow tones.
Its dihalogenides, in particular the dichloride, are expediently used as functional derivatives of fluoranthendicarboxylic acid. B. thionyl chloride is available Lich is 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 110-120 '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 24.7 parts of 4-amino-1,9-anthrapyrimidine in 350 parts of dichlorobenzene is allowed to flow in at 150. After two hours of stirring at 150-160 ', the formation of the dye has ended. 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 |
---|---|---|---|
CH219414T | 1939-01-19 | ||
CH224882T | 1939-01-19 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH224882A true CH224882A (en) | 1942-12-15 |
Family
ID=25726264
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH224882D CH224882A (en) | 1939-01-19 | 1939-01-19 | Process for the production of a vat dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH224882A (en) |
-
1939
- 1939-01-19 CH CH224882D patent/CH224882A/en unknown
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