CH103142A - Process for the production of a new indigoid dye. - Google Patents
Process for the production of a new indigoid dye.Info
- Publication number
- CH103142A CH103142A CH103142DA CH103142A CH 103142 A CH103142 A CH 103142A CH 103142D A CH103142D A CH 103142DA CH 103142 A CH103142 A CH 103142A
- Authority
- CH
- Switzerland
- Prior art keywords
- production
- new
- indigoid dye
- dye
- brown
- 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
- C09B7/00—Indigoid dyes
- C09B7/12—Other thionaphthene indigos
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
Verfahren zur Herstellung eines neuen indigoiden Farbstoffes. Es wurde gefunden, dass man einen neuen indigoiden Farbstoff erhält, wenn man das 5-Chlor-2 . 1-thionaphthisatin, welches durch Kondensieren von 5-Chlor-2-thionaphthol mit Oxalylchlorid erhalten werden kann, mit Ace- naphthenon kondensiert.
Der neue Farbstoff stellt ein braunes Pul ver dar und löst sich in konz. Schwefelsäure mit blauer Farbe. Er bildet eine gelbbraune Küpe und färbt Baumwolle sehr echt in reinen braunen Nuancen.
<I>Beispiel:</I> 248,5 Teile 5-Chlor-2 . 1-thionaphthisatin, 168 Teile Acenaphthenon und 200 Teile Zink chlorid werden in 2000 Teilen Chlorbenzol mehrere Stunden rückfliessend gekocht. Nach dem Erkalten wird filtriert; der ausgeschie dene Farbstoff mit Alkohol gewaschen und getrocknet.
Process for the production of a new indigoid dye. It has been found that a new indigoid dye is obtained if the 5-chloro-2. 1-thionaphthisatin, which can be obtained by condensing 5-chloro-2-thionaphthol with oxalyl chloride, condensed with acenaphthenone.
The new dye is a brown powder and dissolves in conc. Sulfuric acid of blue color. It forms a yellow-brown vat and dyes cotton very realistically in pure brown shades.
<I> Example: </I> 248.5 parts of 5-chloro-2. 1-thionaphthisatin, 168 parts of acenaphthenone and 200 parts of zinc chloride are refluxed for several hours in 2000 parts of chlorobenzene. After cooling, it is filtered; the excreted dye washed with alcohol and dried.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH100705T | 1922-11-18 | ||
CH103142T | 1922-12-07 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH103142A true CH103142A (en) | 1924-01-16 |
Family
ID=25705823
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH103142D CH103142A (en) | 1922-11-18 | 1922-12-07 | Process for the production of a new indigoid dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH103142A (en) |
-
1922
- 1922-12-07 CH CH103142D patent/CH103142A/en unknown
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