CH127701A - Process for the preparation of a ring ketone of the aromatic series. - Google Patents
Process for the preparation of a ring ketone of the aromatic series.Info
- Publication number
- CH127701A CH127701A CH127701DA CH127701A CH 127701 A CH127701 A CH 127701A CH 127701D A CH127701D A CH 127701DA CH 127701 A CH127701 A CH 127701A
- Authority
- CH
- Switzerland
- Prior art keywords
- preparation
- aromatic series
- ring ketone
- ring
- ketone
- Prior art date
Links
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- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Darstellung eines Ringketons der aromatischen Reihe. Gegenstand dieses Patentes ist ein Ver fahren zur Darstellung eines Ringketons der aromatischen Reihe von nachstehender For mel:
EMI0001.0004
welches dadurch gekennzeichnet ist, dass man ,B-Chlorpropionylchlorid mit a-Methylnaph- talin und Aluminiumchlorid kondensiert und das erhaltene Kondensationsprodukt mit konzentrierter Schwefelsäure erwärmt. Das Produkt soll zur Herstellung von Farbstoffen Verwendung finden.
<I>Beispiel:</I> Eine Lösung von 14,2 Gewichtsteilen a- Methylnaphtalin und 12,7 Gewichtsteilen ,B- Chlorpropionylchlorid wird unter Kühlung mit Eiswasser zu einer Aufschlemmung von 30 Gewichtsteilen Aluminiumchlorid in 100 Raumteilen Schwefelkohlenstoff nach und nach gegeben. Nach Beendigung der Um setzung wird mit Eis und Salzsäure versetzt und die wässerige Flüssigkeit ausgeäthert. Der Ätherauszug wird mit der Schwefel kohlenstofflösung vereinigt und abgedampft. Es hinterbleibt eine Kristallmasse, die aus Ligroin umkristallisiert werden kann.
Das so erhaltene 1- Methyl - (ss - Chlorpropionyl) -4- naphtalin schmilzt bei<B>60'.</B> Wird es in konzentrierter Schwefelsäure gelöst und eine halbe Stunde lang auf dem Wasserbade er hitzt, so entweicht Salzsäure, und beim Ein giessen in Wasser scheidet sich das 5-Methyl- 6. 7-benzo-l-indanon aus, das bei 133 schmilzt.
Process for the preparation of a ring ketone of the aromatic series. The subject of this patent is a process for the preparation of a ring ketone of the aromatic series of the following formula:
EMI0001.0004
which is characterized in that B-chloropropionyl chloride is condensed with α-methylnaphthalene and aluminum chloride and the condensation product obtained is heated with concentrated sulfuric acid. The product is intended to be used for the manufacture of dyes.
<I> Example: </I> A solution of 14.2 parts by weight of a-methylnaphthalene and 12.7 parts by weight of B-chloropropionyl chloride is gradually added to a slurry of 30 parts by weight of aluminum chloride in 100 parts by volume of carbon disulfide while cooling with ice water. When the reaction is complete, ice and hydrochloric acid are added and the aqueous liquid is extracted with ether. The ether extract is combined with the carbon disulfide solution and evaporated. What remains is a mass of crystals that can be recrystallized from ligroin.
The 1- methyl - (ss - chloropropionyl) -4- naphthalene obtained in this way melts at <B> 60 '. </B> If it is dissolved in concentrated sulfuric acid and heated for half an hour in the water bath, hydrochloric acid escapes, and when pouring into water, the 5-methyl-6,7-benzo-l-indanone separates out, which melts at 133.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE127701X | 1926-03-26 | ||
CH126404T | 1927-03-14 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH127701A true CH127701A (en) | 1928-09-01 |
Family
ID=25710649
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH127701D CH127701A (en) | 1926-03-26 | 1927-03-14 | Process for the preparation of a ring ketone of the aromatic series. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH127701A (en) |
-
1927
- 1927-03-14 CH CH127701D patent/CH127701A/en unknown
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