CH168023A - Process for the production of a new anthraquinone derivative. - Google Patents
Process for the production of a new anthraquinone derivative.Info
- Publication number
- CH168023A CH168023A CH168023DA CH168023A CH 168023 A CH168023 A CH 168023A CH 168023D A CH168023D A CH 168023DA CH 168023 A CH168023 A CH 168023A
- Authority
- CH
- Switzerland
- Prior art keywords
- production
- anthraquinone derivative
- new anthraquinone
- oxyethylamino
- 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
- 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
- C09B1/26—Dyes with amino groups substituted by hydrocarbon radicals
- C09B1/32—Dyes with amino groups substituted by hydrocarbon radicals substituted by aryl groups
- C09B1/325—Dyes with no other substituents than the amino groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
verfahren zur Herstellung eines neuen Anthrachinonderivates. Es wurde gefunden, dass man ein neues Anthrachinonderivat erhält, wenn man 1-ss Oxyäthylamino-4-methoxyanthrachinon mit Anilin umsetzt, wobei 1 Mol Anilin mit einem Mol des Anthrachinonderivates reagiert.
Der Farbstoff bildet ein dunkles Pulver, löst sich in organischen Lösungsmitteln mit blauer Farbe und färbt Acetatseide nach ge eigneter. Verpastung in reinen blauen Tönen. Durch Sulfieren erhält man einen wertvollen Wollfarbstoff.
<I>Beispiel:</I> 63 Teile 1-p-Oxyäthylamino-4-methoxy- anthrachinon werden in 250 Teilen Anilin ca. 42 Stunden auf 160-180<B>'</B>erwärmt. Man fällt mit 350 Teilen Methylalkohol und erhält in vorzüglicher Reinheit ein Produkt, welches Acetatseide nach geeigneter Verpastung in reinen, blauen Tönen färbt.
process for the production of a new anthraquinone derivative. It has been found that a new anthraquinone derivative is obtained if 1-ss oxyethylamino-4-methoxyanthraquinone is reacted with aniline, 1 mol of aniline reacting with one mol of the anthraquinone derivative.
The dye forms a dark powder, dissolves in organic solvents with a blue color and dyes acetate silk as appropriate. Pasting in pure blue tones. A valuable wool dye is obtained by sulfating.
<I> Example: </I> 63 parts of 1-p-oxyethylamino-4-methoxy-anthraquinone are heated in 250 parts of aniline for about 42 hours to 160-180 <B> '</B>. It is precipitated with 350 parts of methyl alcohol and a product is obtained in excellent purity which, after suitable pasting, dyes acetate silk in pure, blue shades.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH168023T | 1932-09-20 | ||
CH166223T | 1934-02-06 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH168023A true CH168023A (en) | 1934-03-15 |
Family
ID=25718254
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH168023D CH168023A (en) | 1932-09-20 | 1932-09-20 | Process for the production of a new anthraquinone derivative. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH168023A (en) |
-
1932
- 1932-09-20 CH CH168023D patent/CH168023A/en unknown
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