CH131500A - Process for the preparation of a dye intermediate of the benzanthrone series. - Google Patents
Process for the preparation of a dye intermediate of the benzanthrone series.Info
- Publication number
- CH131500A CH131500A CH131500DA CH131500A CH 131500 A CH131500 A CH 131500A CH 131500D A CH131500D A CH 131500DA CH 131500 A CH131500 A CH 131500A
- Authority
- CH
- Switzerland
- Prior art keywords
- preparation
- dye intermediate
- bzl
- sulfide
- benzanthrone series
- Prior art date
Links
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Darstellung eines Farbstoffzwischenproduktes der Benzanthronreihe. Gegenstand -dieser Erfindung ist ein Ver- ehinonylamino - Bz 1- Bz 1' - benzauthronyl- fahren zur Darstellung eines Di-a-antlira- Sulfids: .
EMI0001.0008
welches dadurch gekennzeichnet ist, dass man 6 . 6'-Diamino-Bz 1'-benzanthronylsulfi:d mit a-Chloranthraehinon bei höherer Tem peratur kondensiert.
Beispiel: In 50 Gewichtsteile Nitrobenzol werden :@ C T (,-,vielitsteile 6. 6'-1)iamino-Bzl-Bzl'-benz- anthronyIsulfid. 6 Gewichtsteile a-Chloran- thrachinon, 4 Gewichtsteile wasserfreies Iia- liumkarbonat und 0,2 Gewichtsteile Kupfer- ehlori@d verrührt.
Dieses Gemisch wird lang sam auf 180 bis 190 erhitzt und bei dieser Temperatur belassen, bis sich keine Aus gangsmaterialien mehr nachweisen lassen. Nach dem Erkalten wird abgesaugt, mit Aethylalkohol zur Entfernung des Lösungs mittels und mit Wasser zur Beseitigung der Salze gewaschen. Es hinterbleibt das Di-a- anthraehinony lamino - Bz-1 - Bz 1' - benzan- thronylsulfid als ein rotbraunes Pulver, das sich in konzentrierter Salzsäure mit grüner Farbe löst.
Process for the preparation of a dye intermediate of the benzanthrone series. The subject of this invention is a ver ehinonylamino - Bz 1- Bz 1 '- benzauthronyl- drive for the preparation of a di-a-antlira sulfide:.
EMI0001.0008
which is characterized by the fact that 6. 6'-Diamino-Bz 1'-benzanthronylsulfi: d condensed with a-chloranthraehinone at a higher temperature.
Example: In 50 parts by weight of nitrobenzene: @ C T (, -, many parts 6. 6'-1) iamino-Bzl-Bzl'-benz-anthronyisulfide. 6 parts by weight of a-chloranothrachinone, 4 parts by weight of anhydrous iialium carbonate and 0.2 part by weight of copper-ehlori®d were stirred.
This mixture is slowly heated to 180 to 190 and left at this temperature until no more starting materials can be detected. After cooling, it is filtered off with suction, washed with ethyl alcohol to remove the solvent and with water to remove the salts. What remains is the di-a-anthraehinony lamino - Bz-1 - Bz 1 '- benzanthronyl sulfide as a red-brown powder that dissolves in concentrated hydrochloric acid with a green color.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE131500X | 1926-08-02 | ||
CH130151T | 1927-08-01 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH131500A true CH131500A (en) | 1929-02-15 |
Family
ID=25711369
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH131500D CH131500A (en) | 1926-08-02 | 1927-08-01 | Process for the preparation of a dye intermediate of the benzanthrone series. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH131500A (en) |
-
1927
- 1927-08-01 CH CH131500D patent/CH131500A/en unknown
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