CH170933A - Process for the preparation of a 1-oxyalkylamino-4-arylaminoanthraquinone. - Google Patents
Process for the preparation of a 1-oxyalkylamino-4-arylaminoanthraquinone.Info
- Publication number
- CH170933A CH170933A CH170933DA CH170933A CH 170933 A CH170933 A CH 170933A CH 170933D A CH170933D A CH 170933DA CH 170933 A CH170933 A CH 170933A
- Authority
- CH
- Switzerland
- Prior art keywords
- preparation
- parts
- oxyalkylamino
- mol
- arylaminoanthraquinone
- 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
Zusatzpatent zum Hauptpatent Nr. 166223. Verfahren zur Herstellung eines 1-Oxyalkylamino-4-arylitminoanthrachinons. Es wurde gefunden, dass man ein 1-Oxyal- kylarnirio-4-ai#ylamirioarithrachinon erhalten kann, wenn man auf 1 Mol Leuko-1.4-di-(ss- oxyäthylamino)-anthrachinon 1 Alol 1.4-Di- aminobenzol einwirken lässt und das so er haltene Kondensationsprodukt oxydiert.
Die Oxydation kann durchgeführt werden, indem das abgeschiedene Kondensationspro dukt in einem besonderen Arbeitsgang oxy diert wird; man kann auch das Oxydations mittel während der Kondensation zugeben, es findet dann Oxydation unmittelbar nach Kon densation statt.
Das 1-ss-Oxyäthylamino-4-p-phenylendi- aminoanthrachinon bildet ein dunkles Pulver, das sich in llssigsäirreäthylester mit grüner Farbe löst. Nach geeigneter Verpastung färbt es Acetatkunstseide in vollen und echten grünen Tönen.
<I>Beispiel 1:</I> 6 Teile Leuko-1.4-di(ss-oxyäthylamino)- anthrachinon werden in 30 Teilen Äthanol mit 2 Teilen p-Phenylendiamin und 1 Teil p-Phe- nylendiaminchlorhydrat einige Stunden zum Sieden erhitzt. Das gebildete Produkt wird filtriert und in üblicher Weise oxydiert. <I>Beispiel 2:</I> 8 Teile Leuko-1.4-di(ss-oxyäthylamino)- anthrachinon werden in 35 Teilen Methanol mit 3 Teilen 1.4-Diaminobenzol, 0,7 Teilen Natriumchlorat und 2 Teilen Borsäure mehrere Stunden auf 65 erhitzt.
Man filtriert kalt, wäscht mit Methanol und Wasser und erhält in guter Ausbeute und Reinheit 1-p-Oxyäthyl- amino-4-p-pheriylendiaminoanthrachirion.
Additional patent to main patent No. 166223. Process for the preparation of a 1-oxyalkylamino-4-arylitminoanthraquinone. It has been found that a 1-oxyalkylarnirio-4-ai # ylamirioarithraquinone can be obtained if 1 mol of leuco-1,4-di- (ss- oxyäthylamino) -anthraquinone 1 alol 1,4-diaminobenzene is allowed to act and that so he obtained condensation product is oxidized.
The oxidation can be carried out by the deposited condensation product is oxidized in a special operation; you can also add the oxidizing agent during the condensation, then oxidation takes place immediately after the condensation.
The 1-ss-oxyethylamino-4-p-phenylenediaminanthraquinone forms a dark powder which dissolves in ethyl acetate with a green color. After suitable pasting, it dyes acetate artificial silk in full and real green tones.
<I> Example 1: </I> 6 parts of leuco-1,4-di (ss-oxyethylamino) anthraquinone are heated to boiling for a few hours in 30 parts of ethanol with 2 parts of p-phenylenediamine and 1 part of p-phenylenediamine chlorohydrate. The product formed is filtered and oxidized in the usual way. Example 2: 8 parts of leuco-1,4-di (ss-oxyethylamino) anthraquinone are heated to 65 for several hours in 35 parts of methanol with 3 parts of 1,4-diaminobenzene, 0.7 parts of sodium chlorate and 2 parts of boric acid .
It is filtered cold, washed with methanol and water and 1-p-oxyethylamino-4-p-pheriylenediaminoanthrachirione is obtained in good yield and purity.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH170933T | 1933-04-08 | ||
CH166223T | 1934-02-06 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH170933A true CH170933A (en) | 1934-07-31 |
Family
ID=25718257
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH170933D CH170933A (en) | 1933-04-08 | 1933-04-08 | Process for the preparation of a 1-oxyalkylamino-4-arylaminoanthraquinone. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH170933A (en) |
-
1933
- 1933-04-08 CH CH170933D patent/CH170933A/en unknown
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