CH143262A - Process for the preparation of a compound with a hydrogenated ring system. - Google Patents
Process for the preparation of a compound with a hydrogenated ring system.Info
- Publication number
- CH143262A CH143262A CH143262DA CH143262A CH 143262 A CH143262 A CH 143262A CH 143262D A CH143262D A CH 143262DA CH 143262 A CH143262 A CH 143262A
- Authority
- CH
- Switzerland
- Prior art keywords
- preparation
- compound
- ring system
- hydrogenated ring
- hydrogenated
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C47/00—Compounds having —CHO groups
- C07C47/38—Unsaturated compounds having —CHO groups bound to carbon atoms of rings other than six—membered aromatic rings
- C07C47/42—Unsaturated compounds having —CHO groups bound to carbon atoms of rings other than six—membered aromatic rings with a six-membered ring
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Darstellung einer Verbindung mit; hydriertem Ringsystem. Gegenstand dieses Zusatzpatentes ist ein Verfahren zur Darstellung eines hydrierten Tetramethyl-anthrachinons, welches dadurch gekennzeichnet ist, dass man Benzochinon mit 1 . 3-Dimethyl-butadien kondensiert. Die neue Verbindung soll zur Herstellung von Farb stoffen Verwendung finden.
<I>Beispiel:</I> i; Gewichtsteile Benzochinon werden mit 5 Volumenteilen 1 .3-Dimethyl-butadien eine Stunde auf dem Wasserbad am Rückfluss- kühler erhitzt. Nach dem Erkalten kristalli siert das neue Produkt aus und wird durch Absaugen und Nachwaschen mit Petroläther isoliert. Es schmilzt roh bei 186-1881 C. Aus Eisessig umkristallisiert, erhält man die Verbindung in weissen Nadeln vom Schmelz punkt 194 C.
Method for representing a connection with; hydrogenated ring system. The subject of this additional patent is a process for the preparation of a hydrogenated tetramethyl-anthraquinone, which is characterized in that benzoquinone with 1. 3-dimethyl-butadiene condensed. The new compound will be used to manufacture dyes.
<I> Example: </I> i; Parts by weight of benzoquinone are heated with 5 parts by volume of 1,3-dimethylbutadiene for one hour on a water bath at a reflux condenser. After cooling, the new product crystallizes out and is isolated by suction and washing with petroleum ether. It melts raw at 186-1881 C. Recrystallized from glacial acetic acid, the compound is obtained in white needles with a melting point of 194 C.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH143262T | 1929-01-21 | ||
CH141523T | 1930-08-15 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH143262A true CH143262A (en) | 1930-10-31 |
Family
ID=25713728
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH143262D CH143262A (en) | 1929-01-21 | 1929-01-21 | Process for the preparation of a compound with a hydrogenated ring system. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH143262A (en) |
-
1929
- 1929-01-21 CH CH143262D patent/CH143262A/en unknown
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