DE365902C - Process for the representation of dyes - Google Patents
Process for the representation of dyesInfo
- Publication number
- DE365902C DE365902C DEA33151D DEA0033151D DE365902C DE 365902 C DE365902 C DE 365902C DE A33151 D DEA33151 D DE A33151D DE A0033151 D DEA0033151 D DE A0033151D DE 365902 C DE365902 C DE 365902C
- Authority
- DE
- Germany
- Prior art keywords
- naphthoquinone
- dichloro
- dyes
- representation
- condensation
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
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
- C09B17/00—Azine dyes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Darstellung von Farbstoffen. Es wurde gefunden, daß als Pigmente wie als Küpenfarbstoffe von hervorragenden Echtheitseigenschaften benutzbare Verbindungen erhalten werden, wenn man die aus 2 - 3-Dichlor-i - 4-naphthochinon durch Kondensation mit o-Diaminen erhältlichen Eurhodole (vgl. Z i n c k e , Annalen 286, 56) mit 2 # 3-Dichlori - 4-naphthochinon bei Gegenwart von Metallen und salzsäurebindenden Mitteln erhitzt. B eispiel. 27 Teile Eurhodol aus 2 - 3-Dichlor-i - 4-naphthochinon und i-2-Diaminobenzol werden mit 23 Teilen 2- 3-Dichlor-i -4-naphthochinon, iSTeilen wasserfreiem Natriumacetat, i2Teilen Kupferbronze und 8oo Teilen Äthylbenzol einige Stunden gekocht. Darauf wird das Lösungsmittel mit Dampf abgeblasen und das Reaktionsprodukt mit verdünnter Natronlauge ausgekocht. Der gelbliche Rückstand wird durch Umlösen aus alkalischer Hvdrosulfit-Lösung von Kupfer befreit. Der so erhaltene Farbstoff bildet ein hellgelbes Pulver und nach dem Umkristallisieren aus Nitrobenzol gelbe Nadeln vom Schmelzpunkt 325°.Process for the representation of dyes. It was found that useful as pigments as well as vat dyes with excellent fastness properties Compounds are obtained when one of the 2 - 3-dichloro-i - 4-naphthoquinone Eurhodols obtainable by condensation with o-diamines (cf. Zi n c k e, Annalen 286, 56) with 2 # 3-dichloro - 4-naphthoquinone in the presence of metals and hydrochloric acid binding agents Means heated. Example. 27 parts of Eurhodol from 2 - 3-dichloro-i - 4-naphthoquinone and i-2-diaminobenzene are divided with 23 parts of 2- 3-dichloro-i -4-naphthoquinone anhydrous sodium acetate, i2 parts copper bronze and 800 parts ethylbenzene some Cooked for hours. The solvent is then blown off with steam and the reaction product boiled with dilute sodium hydroxide solution. The yellowish residue is dissolved by dissolving freed from copper from alkaline hydrogen sulfite solution. The dye thus obtained forms a light yellow powder and, after recrystallization from nitrobenzene, yellow Needles with a melting point of 325 °.
In ähnlicher Weise verläuft die Reaktion bei der Kondensation analoger Verbindungen. So erhält man z. B. durch Kondensation von 2 - 3-Dichlor-i - 4-naphthochinon mit dem Eurhod o1 aus 2 - 3-Dichlor-i - q:-rnaphthochinon und i - 2-Diaminonaphthalin einen orangegelben Farbstoff.In a similar way, the reaction in the condensation proceeds more analogously Links. So you get z. B. by condensation of 2 - 3-dichloro-i - 4-naphthoquinone with the Eurhod o1 from 2 - 3-dichloro-i - q: -naphthoquinone and i - 2-diaminonaphthalene an orange-yellow dye.
Claims (1)
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEA33151D DE365902C (en) | 1920-03-08 | 1920-03-08 | Process for the representation of dyes |
DEA33249D DE368168C (en) | 1920-03-08 | 1920-04-07 | Process for the representation of dyes |
DEA33588D DE368170C (en) | 1920-03-08 | 1920-06-15 | Process for the representation of dyes |
DEA33587D DE368169C (en) | 1920-03-08 | 1920-06-15 | Process for the representation of dyes |
DEA34423D DE368171C (en) | 1920-03-08 | 1920-11-25 | Process for the representation of dyes |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEA33151D DE365902C (en) | 1920-03-08 | 1920-03-08 | Process for the representation of dyes |
Publications (1)
Publication Number | Publication Date |
---|---|
DE365902C true DE365902C (en) | 1922-12-23 |
Family
ID=6928037
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DEA33151D Expired DE365902C (en) | 1920-03-08 | 1920-03-08 | Process for the representation of dyes |
Country Status (1)
Country | Link |
---|---|
DE (1) | DE365902C (en) |
-
1920
- 1920-03-08 DE DEA33151D patent/DE365902C/en not_active Expired
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