AT51203B - Process for the preparation of β-β-dianthraquinonylureas. - Google Patents
Process for the preparation of β-β-dianthraquinonylureas.Info
- Publication number
- AT51203B AT51203B AT51203DA AT51203B AT 51203 B AT51203 B AT 51203B AT 51203D A AT51203D A AT 51203DA AT 51203 B AT51203 B AT 51203B
- Authority
- AT
- Austria
- Prior art keywords
- dianthraquinonylureas
- preparation
- desc
- dianthraquinonylurea
- aminoanthraquinone
- Prior art date
Links
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
<Desc/Clms Page number 1>
Verfahren zur Herstellung von ss-ss-Dianthrachinonylharnstoffen.
In weiterer Ausbildung des Verfahrens des Stammpatentes Nr. 47522 wurde gefunden, dass, wenn man 2 Mol. ss-Aminoanthrachinon mit 1 Mol. Chlorkohlensäureäthyl- äther in einem hochsiedenden Lösungsmittel wie z. B. Naphtalin, erhitzt, man direkt den ss-ss-Dianthrachinonylharnstoff in glatter Weise in einer Operation erhält. Die Reaktion verläuft so, dass sich zunächst das in der deutschen Patentschrift Nr 16741 () beschriebene ss-Anthrachinonylurethan bildet, welches sich gemäss den Angaben der Stammpatentschrift Nr. 47522 mit einem weiteren Molekül -Aminoanthrachinon zum ss-ss-Dianthrachinonylharnstoff umsetzt.
EMI1.1
Verwendet man statt Naphtalin als Lösungsmittel Nitrobenzol, so muss entsprechend länger erhitzt werden.
**WARNUNG** Ende DESC Feld kannt Anfang CLMS uberlappen**.
<Desc / Clms Page number 1>
Process for the preparation of ss-ss-dianthraquinonylureas.
In a further development of the process of the parent patent no. 47522 it was found that if 2 mol. Ss-aminoanthraquinone with 1 mol. Chlorocarbonic acid ethyl ether in a high-boiling solvent such as. B. naphthalene heated, the ss-ss-dianthraquinonylurea is obtained directly in one operation in a smooth manner. The reaction proceeds in such a way that the ss-anthraquinonyl urea described in German patent specification No. 16741 () is initially formed, which, according to the information in parent patent specification No. 47522, reacts with another molecule -aminoanthraquinone to form ss-ss-dianthraquinonylurea.
EMI1.1
If nitrobenzene is used as a solvent instead of naphthalene, the heating must be correspondingly longer.
** WARNING ** End of DESC field may overlap beginning of CLMS **.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE47522X | 1909-02-01 | ||
DE51203X | 1909-03-01 |
Publications (1)
Publication Number | Publication Date |
---|---|
AT51203B true AT51203B (en) | 1911-12-11 |
Family
ID=25749055
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AT51203D AT51203B (en) | 1909-02-01 | 1910-02-07 | Process for the preparation of β-β-dianthraquinonylureas. |
Country Status (1)
Country | Link |
---|---|
AT (1) | AT51203B (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE102006006301B4 (en) | 2006-02-10 | 2013-03-07 | Hiwin Technologies Corp. | Suspension of a threaded spindle |
-
1910
- 1910-02-07 AT AT51203D patent/AT51203B/en active
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE102006006301B4 (en) | 2006-02-10 | 2013-03-07 | Hiwin Technologies Corp. | Suspension of a threaded spindle |
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