CH150161A - Process for the preparation of an arylacetic acid. - Google Patents
Process for the preparation of an arylacetic acid.Info
- Publication number
- CH150161A CH150161A CH150161DA CH150161A CH 150161 A CH150161 A CH 150161A CH 150161D A CH150161D A CH 150161DA CH 150161 A CH150161 A CH 150161A
- Authority
- CH
- Switzerland
- Prior art keywords
- preparation
- acid
- acenaphthyl
- acetic acid
- arylacetic acid
- Prior art date
Links
Description
Verfahren zur Darstellung einer Arylessigsäure. Gegenstand dieses Zusatzpatentes ist ein Verfahren zur Darstellung von Ace- naphtyl-ä-essigsäure, welches darin besteht, dass man Acenaphten und Monochloressig- säure aufeinander einwirken lässt; vorzugs weise nimmt man die Reaktion bei erhöhter Temperatur vor.
<I>Beispiel:</I> 20-0 Gewichtsteile Acenaphten werden mit 250 Gewichtsteilen Monochloressigsäure unter Rühren<B>60</B> Stunden lang auf <B>175 '</B> erwärmt. Nach dem Abkühlen zerreibt man die Masse in kaltem Wasser, saugt ab und zieht den Rückstand mit etwa 3%iger Na tronlauge aus. Aus der filtrierten alkalischen Lösung fällt durch Ansäuern mit verdünn ter Mineralsäure die Acenaphtylessigsäure als graubrauner Niederschlag aus. Man kann aueli die Aufarbeitung so vornehmen, dass man nach dem Ausziehen mit Wasser den Rückstand trocknet und mit Äther extra hiert.
Nach dem Verdunsten des Äthers wird die Säure entweder aus --LUethylalkohol um kristallisiert oder im Vakuum destilliert, wobei sie bei<B>9</B> mm um etwa<B>180'</B> überaeht Die Acenaphtyl-5-essigsäure kristallisiert in farblosen Prismen und schmilzt nach vor herigem Sintern bei<B>187 ' C.</B>
Neben dieser als Hauptprodukt erhalte nen Acenaphtyl-5-essigsäure entsteht noch eine isomere Säure von niedrigerem Schmelz punkt in kleiner Menge. Die Verbindung soll als Zwischenprodukt für die Farbstoff- herstellung Verwendung finden.
Process for the preparation of an arylacetic acid. The subject of this additional patent is a process for the preparation of acenaphthyl-a-acetic acid, which consists in allowing acenaphthene and monochloroacetic acid to act on one another; preferably, the reaction is carried out at an elevated temperature.
<I> Example: </I> 20-0 parts by weight of acenaphthene are heated with 250 parts by weight of monochloroacetic acid while stirring for <B> 60 </B> hours to <B> 175 '</B>. After cooling, the mass is ground in cold water, filtered off with suction and the residue is extracted with about 3% strength sodium hydroxide solution. Acenaphthylacetic acid precipitates out of the filtered alkaline solution as a gray-brown precipitate by acidification with dilute mineral acid. The work-up can also be carried out in such a way that, after being drawn off with water, the residue is dried and extracted with ether.
After the ether has evaporated, the acid is either recrystallized from --LUethyl alcohol or distilled in vacuo, where it overtakes about <B> 180 '</B> at <B> 9 </B> mm. Acenaphthyl-5-acetic acid crystallizes in colorless prisms and melts at <B> 187 'C. </B> after previous sintering
In addition to this acenaphthyl-5-acetic acid obtained as the main product, an isomeric acid with a lower melting point is also formed in small quantities. The compound is said to be used as an intermediate for dye production.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE150161X | 1929-02-01 | ||
CH146854T | 1930-01-23 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH150161A true CH150161A (en) | 1931-10-15 |
Family
ID=25714933
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH150161D CH150161A (en) | 1929-02-01 | 1930-01-23 | Process for the preparation of an arylacetic acid. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH150161A (en) |
-
1930
- 1930-01-23 CH CH150161D patent/CH150161A/en unknown
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