CH121501A - Process for the production of a new vat dye. - Google Patents
Process for the production of a new vat dye.Info
- Publication number
- CH121501A CH121501A CH121501DA CH121501A CH 121501 A CH121501 A CH 121501A CH 121501D A CH121501D A CH 121501DA CH 121501 A CH121501 A CH 121501A
- Authority
- CH
- Switzerland
- Prior art keywords
- production
- new
- vat dye
- new vat
- 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
- C09B7/00—Indigoid dyes
- C09B7/06—Indone-thionapthene indigos
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
Verfahren zur Herstellung eines neuen güpenfarbstoffes. Es wurde gefunden, dass man-einen neuen Küpenfarbstoff erhält, wenn man 1 Mol. 4.6- Dimethyl-3-oxythionaphten mit einem Molekül 7-Chlorisatin kondensiert und das so erhaltene Produkt bromiert. Der neue Farbstoff bildet ein rotes Pulver, löst sich in konzentrierter Schwefelsäure mit grüner Farbe und gibt mit Hydrosulfit und Natronlauge eine blass gelbe Küpe,
aus welcher Baumwolle echt blaustichig rosa gefärbt wird.
Beispiel: 178 Teile 4.6-Dimethyl-3-oxythionaphten und 181,5 Teile 7-Chlorisatin werden in 1800 Teilen Eisessig suspendiert und dann zum Sieden erhitzt. Die Kondensation ist in kurzer Zeit beendigt. Es wird filtriert, mit Alkohol gewaschen und getrocknet.
341,5 Teile des so erhaltenen Produktes werden in 6000 Teile Nitrobenzol eingetragen und mit 176 Teilen Brom versetzt. Während 12 Stunden wird die Reaktionsmasse sich selbst überlassen, hierauf langsam auf 120 bis 130 erwärmt und solange bei dieser Tempe ratur gehalten, bis die Bromwasserstoffent- wicklung beendigt ist. Nach dem Erkalten wird filtriert, mit Alkohol gewaschen und getrocknet.
Process for the production of a new high quality dye. It has been found that a new vat dye is obtained if 1 mol of 4,6-dimethyl-3-oxythionaphthene is condensed with one molecule of 7-chloroisatin and the product thus obtained is brominated. The new dye forms a red powder, dissolves in concentrated sulfuric acid with a green color and, with hydrosulfite and caustic soda, gives a pale yellow vat,
which cotton is dyed with a real bluish pink.
Example: 178 parts of 4,6-dimethyl-3-oxythionaphthene and 181.5 parts of 7-chloroisatin are suspended in 1,800 parts of glacial acetic acid and then heated to the boil. The condensation ends in a short time. It is filtered, washed with alcohol and dried.
341.5 parts of the product thus obtained are introduced into 6000 parts of nitrobenzene, and 176 parts of bromine are added. The reaction mass is left to its own devices for 12 hours, then slowly heated to 120 to 130 and kept at this temperature until the evolution of hydrogen bromide has ceased. After cooling, it is filtered, washed with alcohol and dried.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH121501T | 1925-10-31 | ||
CH118233T | 1926-12-16 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH121501A true CH121501A (en) | 1927-07-01 |
Family
ID=25708986
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH121501D CH121501A (en) | 1925-10-31 | 1925-10-31 | Process for the production of a new vat dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH121501A (en) |
-
1925
- 1925-10-31 CH CH121501D patent/CH121501A/en unknown
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