CH159322A - A process for the manufacture of 3: 3'-dichlorotetrahydrodianthraquinone-1: 2: 2 'tetrasulfuric ester: 1'-dihydroazine. - Google Patents
A process for the manufacture of 3: 3'-dichlorotetrahydrodianthraquinone-1: 2: 2 'tetrasulfuric ester: 1'-dihydroazine.Info
- Publication number
- CH159322A CH159322A CH159322DA CH159322A CH 159322 A CH159322 A CH 159322A CH 159322D A CH159322D A CH 159322DA CH 159322 A CH159322 A CH 159322A
- Authority
- CH
- Switzerland
- Prior art keywords
- tetrasulfuric
- ester
- dihydroazine
- manufacture
- esters
- Prior art date
Links
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- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Procédé de fabrication de l'ester tétrasulfurique de la 3:3'-dichlorotétrahydro- dianthraquinone-1: 2 : 2': 1'-dihydroazine. On sait déjà fabriquer et appliquer des esters sulfuriques des indanthrones réduites, esters que l'on croit être les esters tétrasulfu- riques des tétrahydrodianthraquinone-l :2 2' : l'-azines (dianthrahydroquinone-1 : 2 2' : l'-azines).
On a constaté, selon l'invention, que ces esters tétrasulfuriques des tétrahydrodian- thraquinoneazines peuvent être convertis en de nouveaux esters qui semblent être les es ters tétrasulfuriques des tétrahydrodianthra- quinonedihydroazines. On a également cons taté que des esters tétrasulfuriques peuvent être transformés en encore d'autres nouveaux esters qui semblent être des esters trisulfu- riques et que ces esters trisulfuriques peu vent
être convertis en de nouveaux esters di sulfuriques.
La présente invention est relative à la conversion de l'ester tétrasulfurique de la 3 : 3'-dichlorotétrahydrodianthraquinone-1 2 :92' : l'-azine par réduction en l'ester tétra- sulfurique de la 3:3'-dichlorotétra.hydro- dianthraquinone-1 : 2 : 2' : l'-dihydroazine (3 : 3'-dichlorodianthrahydroquinone-1 : 2 2' : l'-dihydroazine.
L'exemple suivant dans lequel les parties sont en poids explique l'invention sans la li miter. <I>Exemple:</I> 10 parties du sel de potassium de l'ester tétrasulfurique de la. 3 :3'-dichlorotétra.hy- drodianthraquinonea.zine en solution dans 50 parties d'eau sont traitées par 24,5 parties de soude caustique à 20% et 5 parties d'hy- drosulfite de sodium (892%). La liqueur est agitée à 40 C pendant 15 minutes et l'on ajoute alors 20 parties de chlorure de potas sium.
Après refroidissement à 5 . la masse vert foncé est filtrée et lavée sur le filtre avec du chlorure de potassium saturé conte- riant du gaz carbonique et rendu légèrement. alcalin au moyen de carbonate.
A process for the manufacture of 3: 3'-dichlorotetrahydro-dianthraquinone-1: 2: 2 ': 1'-dihydroazine tetrasulfuric ester. It is already known how to make and apply sulfuric esters of reduced indanthrones, esters believed to be the tetrasulfuric esters of tetrahydrodianthraquinone-1: 2 2 ': l'-azines (dianthrahydroquinone-1: 2 2': l'- azines).
It has been found, according to the invention, that these tetrasulfuric esters of tetrahydrodianthraquinoneazines can be converted into new esters which appear to be the tetrasulfuric esters of tetrahydrodianthraquinonedihydroazines. It has also been found that tetrasulfuric esters can be converted to yet other new esters which appear to be trisulfuric esters and that these trisulfuric esters can be converted
be converted into new sulfuric esters.
The present invention relates to the conversion of the tetrasulfuric ester of 3: 3'-dichlorotetrahydrodianthraquinone-1 2: 92 ': l'-azine by reduction to the tetrasulfuric ester of 3: 3'-dichlorotetra. hydro-dianthraquinone-1: 2: 2 ': l'-dihydroazine (3: 3'-dichlorodianthrahydroquinone-1: 2 2': l'-dihydroazine.
The following example in which parts are by weight explains the invention without limiting it. <I> Example: </I> 10 parts of the potassium salt of the tetrasulfuric ester of the. 3: 3'-dichlorotétra.hy- drodianthraquinonea.zine dissolved in 50 parts of water are treated with 24.5 parts of 20% caustic soda and 5 parts of sodium hydrosulphite (892%). The liquor is stirred at 40 C for 15 minutes and then 20 parts of potassium chloride are added.
After cooling to 5. the dark green mass is filtered and washed on the filter with saturated potassium chloride containing carbon dioxide and made lightly. alkaline by means of carbonate.
Claims (1)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB159322X | 1930-06-13 | ||
GB100231X | 1931-02-10 | ||
CH157667T | 1931-06-13 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH159322A true CH159322A (en) | 1932-12-31 |
Family
ID=27177396
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH159322D CH159322A (en) | 1930-06-13 | 1931-06-13 | A process for the manufacture of 3: 3'-dichlorotetrahydrodianthraquinone-1: 2: 2 'tetrasulfuric ester: 1'-dihydroazine. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH159322A (en) |
-
1931
- 1931-06-13 CH CH159322D patent/CH159322A/en unknown
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