CH252953A - Process for the production of a vat dye. - Google Patents
Process for the production of a vat dye.Info
- Publication number
- CH252953A CH252953A CH252953DA CH252953A CH 252953 A CH252953 A CH 252953A CH 252953D A CH252953D A CH 252953DA CH 252953 A CH252953 A CH 252953A
- Authority
- CH
- Switzerland
- Prior art keywords
- acid
- vat dye
- production
- vat
- 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
- C09B5/00—Dyes with an anthracene nucleus condensed with one or more heterocyclic rings with or without carbocyclic rings
- C09B5/24—Dyes with an anthracene nucleus condensed with one or more heterocyclic rings with or without carbocyclic rings the heterocyclic rings being only condensed with an anthraquinone nucleus in 1-2 or 2-3 position
- C09B5/34—Anthraquinone acridones or thioxanthrones
- C09B5/40—Condensation products of benzanthronyl-amino-anthraquinones
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Zusatzpatent zum Hauptpatent Nie 247444. Verfahren zur Herstellung eines Küpenfarbstoffes. Es wurde gefunden, dass ein wertvoller Küpenfarbstoff hergestellt werden kann, wenn man das in alkalischem Medium er balten.e Kondensationsprodukt aus 1-(Bzl- henzanthronylamino) - 5 - aminoanthra.chinon Mit einem Mittel behandelt, das den Rest der
EMI0001.0009
Der. neue Farbstoff ist ein olives Pul- v:
@r, das sich in Schwefelsäure grün löst und :ois rotstichig blauer Küpe Baumwolle oder Wllwolle in gelbstichig oliven Tönen färbt:.
Das dem vorliegenden Verfahren als Aus gangsprodukt dienende alkalische Konden sationsprodukt aus: 1-(Bzl-Benzanthronyl- amino)-5-aminoanthrachinon kann in beka-nn- terWeise erhalten werden, z. B. unter Ver wendung von alkoholischen ÄtzallLa:lilösun- gen bzw. Schmelzen (vergl. französische Pa- ientschriften Nr.697231 und ä96583).
Als Mittel, die den Rest der obigen For mel abgeben, kommen vorzugsweise reak- iionsfähige, funktionelle Derivate der 2,4- Diehlorbenzoesäure, z. Bi., die Säurehaloi- genide und insbes,ondere das Säurechlorid, in Betracht.
Die Behandlung kann in an sich bekann ter ZVeise z. B. durch Erhitzen in indiffe- rentün, vorzugsweise hochsiedenden Lösungs mitteln wie Nitrobenzol, Naphthalin und Diehlorbenzol vorgenommen werden.
Beispiel: ?0 Teile a.lkal. Kondensationsprodukt aus 1- (Bzl-Benzanthronylamino)-5-aminoanthra- chinon werden in 250 Teilen Nitrobenzol mit 30 Teilen 2,4-Dichlorbenzoylchlorid erwärmt und 21 Stunden rückfliessend gekocht. Nach Erkalten wird abgesaugt; der Rückstand wird zuerst mit Nitrobenzol, dann mit Chlorben zol, hierauf mit Alkohol und schliesslich mit Wasser gewaschen und nach Erreichung einer neutralen Reaktion getrocknet.
Additional patent to the main patent Nie 247444. Process for the production of a vat dye. It has been found that a valuable vat dye can be produced if the condensation product of 1- (benzanthronylamino) -5-aminoanthraquinone is treated with an agent that treats the rest of the
EMI0001.0009
Of the. new dye is an olive powder:
@r, which dissolves green in sulfuric acid and: ois reddish-tinged blue vat dyes cotton or wool in yellow-tinged olive tones :.
The alkaline condensation product from: 1- (Bzl-benzanthronyl-amino) -5-aminoanthraquinone, which serves as the starting product for the present process, can be obtained in a known manner, e.g. B. using alcoholic caustic solutions or melts (see French patent publications No. 697231 and 96583).
The agents that release the remainder of the formula above are preferably reactive, functional derivatives of 2,4-dichlorobenzoic acid, eg. Bi., The acid halides and especially the acid chloride, into consideration.
The treatment can be carried out in ZVeise known per se z. B. be made by heating in indifferent, preferably high-boiling solvents such as nitrobenzene, naphthalene and diehlorbenzene.
Example:? 0 parts a.lcal. Condensation product of 1- (Bzl-benzanthronylamino) -5-aminoanthraquinone are heated in 250 parts of nitrobenzene with 30 parts of 2,4-dichlorobenzoyl chloride and refluxed for 21 hours. After cooling down, suction is performed; the residue is washed first with nitrobenzene, then with chlorobenzene, then with alcohol and finally with water and dried after a neutral reaction has been achieved.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH247444T | 1944-09-25 | ||
CH252953T | 1944-09-25 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH252953A true CH252953A (en) | 1948-01-31 |
Family
ID=25729212
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH252953D CH252953A (en) | 1944-09-25 | 1944-09-25 | Process for the production of a vat dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH252953A (en) |
-
1944
- 1944-09-25 CH CH252953D patent/CH252953A/en unknown
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