CH178120A - Process for the production of an indigoid dye. - Google Patents
Process for the production of an indigoid dye.Info
- Publication number
- CH178120A CH178120A CH178120DA CH178120A CH 178120 A CH178120 A CH 178120A CH 178120D A CH178120D A CH 178120DA CH 178120 A CH178120 A CH 178120A
- Authority
- CH
- Switzerland
- Prior art keywords
- production
- dye
- indigoid dye
- methyl
- blackish
- Prior art date
Links
- 238000004519 manufacturing process Methods 0.000 title claims description 3
- 238000000034 method Methods 0.000 title claims description 3
- 239000013078 crystal Substances 0.000 claims description 3
- 239000000843 powder Substances 0.000 claims description 3
- 229920000742 Cotton Polymers 0.000 claims description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 2
- PCKPVGOLPKLUHR-UHFFFAOYSA-N indoxyl Chemical group C1=CC=C2C(O)=CNC2=C1 PCKPVGOLPKLUHR-UHFFFAOYSA-N 0.000 claims 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 6
- 239000000975 dye Substances 0.000 description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- ZEUWWCOQJNSGCH-UHFFFAOYSA-N 7-chloro-4-methyl-1h-indole-2,3-dione Chemical class CC1=CC=C(Cl)C2=C1C(=O)C(=O)N2 ZEUWWCOQJNSGCH-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
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
Zusatzpatent zum Hauptpatent Nr. 176362. Verfahren zur Herstellung eines indigoiden Farbstoffes. Es wurde gefunden, dass man einen indi- goiden Farbstoff erhalten kann, wenn man die reaktionsfähigen a-Derivate :des 4-Methyl- 7-ehlorisatins mit 1.2-Naphththioindoxyl kondensiert.
Der Farbstoff :der Formel
EMI0001.0010
stellt :ein schwärzliches Kristallpulver dar, das & :ieh in konzentrierter Schwefelsäure mit grünblauer Farbe löst und Baumwolle aus oranger Küpe in sehr echten, braunvioletten Tönen färbt.
<I>Beispiel:</I> 19,6 Teile 4-Methyl-7-ehlorisatin werden durch Erwärmen mit 22 Teilen Phosphor penta:chlorid in 30,0 Teilen Chlorbenzol in das 4-Methyl-7-chlorieatin-a-e hlorid verwan delt und mit einer bei 65 bis<B>70'</B> hergestell ten höaung von 20 Teilen 1.2-Naphth- thioindoxyl in 600 Teilen Chlorbenzol ver- einigt. Der als schwärzliches Kristallpulver sich ausseheidende Farbstoff wird filtriert, mit Chlorbenzol, sowie mit Alkohol gewa schen und getrocknet.
Additional patent to main patent No. 176362. Process for the production of an indigoid dye. It has been found that an indigoid dye can be obtained if the reactive α-derivatives of 4-methyl-7-chloroisatin are condensed with 1,2-naphththioindoxyl.
The dye: the formula
EMI0001.0010
represents: a blackish crystal powder which &: ieh dissolves in concentrated sulfuric acid with a green-blue color and dyes cotton from an orange vat in very real, brown-violet tones.
<I> Example: </I> 19.6 parts of 4-methyl-7-ehlorisatin are converted into 4-methyl-7-chlorieatine-ae chloride by heating with 22 parts of phosphorus penta: chloride in 30.0 parts of chlorobenzene and combined with a concentration of 20 parts of 1,2-naphthioindoxyl in 600 parts of chlorobenzene, produced at 65 to 70 '. The dye, which separates out as blackish crystal powder, is filtered, washed with chlorobenzene and alcohol and dried.
Claims (1)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH178120T | 1934-04-20 | ||
| CH176362T | 1934-04-20 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH178120A true CH178120A (en) | 1935-06-30 |
Family
ID=25719844
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH178120D CH178120A (en) | 1934-04-20 | 1934-04-20 | Process for the production of an indigoid dye. |
Country Status (1)
| Country | Link |
|---|---|
| CH (1) | CH178120A (en) |
-
1934
- 1934-04-20 CH CH178120D patent/CH178120A/en unknown
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