CH123739A - Process for the preparation of an indigoid dye. - Google Patents
Process for the preparation of an indigoid dye.Info
- Publication number
- CH123739A CH123739A CH123739DA CH123739A CH 123739 A CH123739 A CH 123739A CH 123739D A CH123739D A CH 123739DA CH 123739 A CH123739 A CH 123739A
- Authority
- CH
- Switzerland
- Prior art keywords
- preparation
- dye
- indigoid dye
- dichloroisatin
- oxy
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 3
- 238000002360 preparation method Methods 0.000 title claims description 3
- 239000000843 powder Substances 0.000 claims description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 2
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 9
- 239000000975 dye Substances 0.000 description 5
- 229920000742 Cotton Polymers 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- UHZYTMXLRWXGPK-UHFFFAOYSA-N phosphorus pentachloride Chemical compound ClP(Cl)(Cl)(Cl)Cl UHZYTMXLRWXGPK-UHFFFAOYSA-N 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000000984 vat dye Substances 0.000 description 1
Landscapes
- Developing Agents For Electrophotography (AREA)
Description
Verfahren zur Darstellung eines indigoiden Farbstoffes. Es wurde gefunden, dass sich 4. 5. 6. 7- Tetrahalogen-3-oxy-l-thionaphten derFormel:
EMI0001.0007
mit zyklischen Diketonen oder deren Sub- stitutionsprodukten oder reaktionsfähigen a- Derivaten zu wertvollen Küpenfarbstoffen kondensieren lässt.
So erhält man bei der Kondensation von 4.5.6.7-Tetrachlor-3- oxy-l-thionaphten mit 5.7-Dichlorisatin-a- chlorid einen Farbstoff von hervorragender Echtheit.
Beispiel Zu einer aus 11 Gewichtsteilen 5 . 7-Di- chlorisatin, 50 Gewichtsteilen Benzol und 11 Gewichtsteilen Phosphorpentachlorid her gestellten Lösung von 5.7-Dichlorisatin-a- chlorid wird eine Aufschlämmung von 15 Gewichtsteilen 4.'5. 6. 7-Tetrachlor-3- oxy-l-thionaphten in 30 Gewichtsteilen Ben zol hinzugesetzt. Nach kurzem Erwärmen ist die Kondensation beendet.
Der abfiltrierte und mit Benzol ausgewaschene Farbstoff färbt auf Baumwolle ein Violett von hervor ragender Echtheit.
Der Farbstoff bildet ein violettes Pulver und löst sich in konzentrierter Schwefelsäure mit blauer Farbe.
Process for the preparation of an indigoid dye. It was found that 4. 5. 6. 7-Tetrahalogen-3-oxy-1-thionaphthene of the formula:
EMI0001.0007
with cyclic diketones or their substitution products or reactive a-derivatives condenses to form valuable vat dyes.
Thus, when 4.5.6.7-tetrachloro-3-oxy-1-thionaphthene is condensed with 5.7-dichloroisatin a-chloride, a dye of excellent fastness is obtained.
Example of one of 11 parts by weight 5. 7-dichloroisatin, 50 parts by weight of benzene and 11 parts by weight of phosphorus pentachloride produced solution of 5.7-dichloroisatin a-chloride is a suspension of 15 parts by weight of 4.'5. 6. 7-tetrachloro-3-oxy-1-thionaphthene in 30 parts by weight of benzene was added. After a short period of heating, the condensation has ended.
The dye which is filtered off and washed out with benzene dyes cotton a violet of excellent fastness.
The dye forms a purple powder and dissolves in concentrated sulfuric acid with a blue color.
Claims (1)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE123739X | 1925-12-04 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH123739A true CH123739A (en) | 1927-12-16 |
Family
ID=5657922
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH123739D CH123739A (en) | 1925-12-04 | 1926-11-29 | Process for the preparation of an indigoid dye. |
Country Status (1)
| Country | Link |
|---|---|
| CH (1) | CH123739A (en) |
-
1926
- 1926-11-29 CH CH123739D patent/CH123739A/en unknown
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