CH190890A - Process for the production of a new intermediate product. - Google Patents
Process for the production of a new intermediate product.Info
- Publication number
- CH190890A CH190890A CH190890DA CH190890A CH 190890 A CH190890 A CH 190890A CH 190890D A CH190890D A CH 190890DA CH 190890 A CH190890 A CH 190890A
- Authority
- CH
- Switzerland
- Prior art keywords
- production
- methyl
- intermediate product
- new intermediate
- red
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/51—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition
- C07C45/54—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition of compounds containing doubly bound oxygen atoms, e.g. esters
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Herstellung eines neuen Zwischenproduktes. Es wurde gefunden, dass man ein neues Zwischenprodukt - das 1-Oxy-6-metbyl-3,4- berrzofiuorenon der Formel
EMI0001.0003
erhält, wenn man das 2-Oxynaphthalin-3- (4'-methyl)-phenylketon mit Kondensations mitteln, wie Alurniniumchlorid, verbackt.
Das 1-Oxy-6-methyl-3,4-benzofluorenon bildet ein rotes, in Wasser unlösliches Pulver, das sich in Ätzalkalien mit violettroter Farbe löst. Es stellt ein wichtiges Zwischenprodukt zur Herstellung von Farbstoffen dar.
Beispiel: 25 Teile 2-Oxynaphthalin-3-(4'-methyl)- phenylketon werden mit 75 Teilen Aluminium chlorid 2 Stunden bei 120-130' und hierauf 1 Stunde bei 140-150 o gerührt. Die dick flüssige Schmelze wird beim Erkalten fest. Sie wird pulverisiert und unter Rühren all mählich in verdünnte Salzsäure eingetragen und einige Zeit gerührt. Das Kondensations produkt wird genutscht, in verdünnter Na tronlauge warm gelöst und von etwaigen Verunreinigungen abfiltriert. Die klare Lösung wird mit 10 o/oiger Salzsäure angesäuert, wo bei das neue Kondensationsprodukt ausfällt. S. P. aus Alkohol 178 .
Process for the production of a new intermediate product. It has been found that a new intermediate - the 1-oxy-6-metbyl-3,4-berrzofiuorenon of the formula
EMI0001.0003
obtained when the 2-oxynaphthalene-3- (4'-methyl) phenyl ketone with condensation agents such as aluminum chloride, baked.
The 1-oxy-6-methyl-3,4-benzofluorenone forms a red, water-insoluble powder, which dissolves in caustic alkalis with a purple-red color. It is an important intermediate in the manufacture of dyes.
Example: 25 parts of 2-oxynaphthalene-3- (4'-methyl) - phenyl ketone are stirred with 75 parts of aluminum chloride for 2 hours at 120-130 ° and then for 1 hour at 140-150 °. The thick liquid melt solidifies when it cools. It is pulverized and gradually added to dilute hydrochloric acid while stirring and stirred for a while. The condensation product is suction filtered, dissolved warm in dilute sodium hydroxide solution and any impurities are filtered off. The clear solution is acidified with 10% hydrochloric acid, whereupon the new condensation product precipitates. S. P. from alcohol 178.
Claims (1)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH190890T | 1935-11-26 | ||
| CH188319T | 1935-11-26 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH190890A true CH190890A (en) | 1937-03-15 |
Family
ID=25721627
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH190890D CH190890A (en) | 1935-11-26 | 1935-11-26 | Process for the production of a new intermediate product. |
Country Status (1)
| Country | Link |
|---|---|
| CH (1) | CH190890A (en) |
-
1935
- 1935-11-26 CH CH190890D patent/CH190890A/en unknown
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