CH143290A - Process for the preparation of a cyclammonium compound. - Google Patents
Process for the preparation of a cyclammonium compound.Info
- Publication number
- CH143290A CH143290A CH143290DA CH143290A CH 143290 A CH143290 A CH 143290A CH 143290D A CH143290D A CH 143290DA CH 143290 A CH143290 A CH 143290A
- Authority
- CH
- Switzerland
- Prior art keywords
- compound
- formula
- cyclammonium
- preparation
- product
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/08—Indoles; Hydrogenated indoles with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to carbon atoms of the hetero ring
-
- 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
- C09B23/00—Methine or polymethine dyes, e.g. cyanine dyes
- C09B23/02—Methine or polymethine dyes, e.g. cyanine dyes the polymethine chain containing an odd number of >CH- or >C[alkyl]- groups
- C09B23/06—Methine or polymethine dyes, e.g. cyanine dyes the polymethine chain containing an odd number of >CH- or >C[alkyl]- groups three >CH- groups, e.g. carbocyanines
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Yerfalireii für lierstellutig einer Cyclainnioniiunverbüidung. Es wurde gefunden, dass man eine Cyclammoniumverbindung erhalten kann, wenn man das Produkt der Formel
EMI0001.0005
in nicht alkalischem Medium mit Uhinonen oxydiert und auf das gebildete Additions- produkt mit. dem ebenfalls entstandenen I-Ivdroeliinon Alkalien einwirken lässt.
. Die hierbei < uisgeschiecleneCyclainmoniuni- verbindung stellt ein in Wasser schwer lösliches, braunes Pulver dar. Dieses bildet dni-cli Behandlung mit Säuren Salze der Formel
EMI0001.0018
die tannierte Baumwolle in blauvioletten Tönen färben.
<I>Beispiel:</I> 448 Teile des Produktes der Formel
EMI0001.0021
werden in 4000 'Geilen Benzol gelöst bezw. suspendiert und unter Rühren <B>66,6</B> Teile Eis essig und 122 Teile Chinon innert ein bis zwei Stunden bei 30 bis 85 zugefügt. Hierauf wird 15 bis 20 Stunden bei ge wöhnlicher Tempera.tür weiter gerührt un < 1 hierauf von den abgeschiedenen metallglän- z(-,
iiden Kristallen abfiltriert. Die Unter- suchung des erhaltenen Produktes lässt ver muten, class ein Additionsprodukt von Hydro- chinon in das 1 . 3 . 3 . L' . 3' . 3' - Hexa- niethyl - 5 . 5' - dinitro - 2 . 2' - streptomono- vil'iylenindoey aninacetat vorliegt. Der Kör per löst sich leicht in heissem Wasser.
Beim Versetzen der wässerigen Lösung mit ver dünnter Natronlauge fällt die Cyelammo- niumverbindung aus.
Yerfalireii for one digit of a Cyclainnioniiunverbünung. It has been found that a cyclammonium compound can be obtained by using the product of the formula
EMI0001.0005
oxidized in a non-alkaline medium with uhinones and on the addition product formed with. the also created I-Ivdroeliinon alkalis can act.
. The cyclainmonium compound described here is a brown powder which is sparingly soluble in water. This forms salts of the formula when treated with acids
EMI0001.0018
dye the tannic cotton in blue-violet tones.
<I> Example: </I> 448 parts of the product of the formula
EMI0001.0021
are dissolved in 4000 'Geile benzene respectively. suspended and with stirring <B> 66.6 </B> parts of glacial vinegar and 122 parts of quinone within one to two hours at 30 to 85 added. Stirring is then continued for 15 to 20 hours at the usual temperature, and the metallic luster (-,
iiden crystals filtered off. Examination of the product obtained suggests that an addition product of hydroquinone in the 1. 3. 3. L '. 3 '. 3 '- hexaniethyl - 5. 5 '- dinitro - 2nd 2 '- streptomonovil'iylenindoey aninacetat is present. The body dissolves easily in hot water.
When the aqueous solution is mixed with dilute sodium hydroxide solution, the cyelammonium compound precipitates.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH143290T | 1928-06-21 | ||
CH141551T | 1928-06-21 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH143290A true CH143290A (en) | 1930-10-31 |
Family
ID=25713895
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH143290D CH143290A (en) | 1928-06-21 | 1928-06-21 | Process for the preparation of a cyclammonium compound. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH143290A (en) |
-
1928
- 1928-06-21 CH CH143290D patent/CH143290A/en unknown
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