CH173735A - Process for the preparation of a derivative of p-nitrobenzoyl acetic acid. - Google Patents
Process for the preparation of a derivative of p-nitrobenzoyl acetic acid.Info
- Publication number
- CH173735A CH173735A CH173735DA CH173735A CH 173735 A CH173735 A CH 173735A CH 173735D A CH173735D A CH 173735DA CH 173735 A CH173735 A CH 173735A
- Authority
- CH
- Switzerland
- Prior art keywords
- acetic acid
- derivative
- nitrobenzoyl
- preparation
- nitrobenzoyl acetic
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
- C07C233/01—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C233/12—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by halogen atoms or by nitro or nitroso groups
Description
Verfahren zur Herstellung eines Derivates der p-Nitrobenzoylessigsäure. Es wurde gefunden, dass man ein neues Derivat der p-Nitrobenzoylessigsäure erhält, wenn man auf 1 Mol p-Nitroberizoylessigester 1 Mol p-Aminobenzoylanilin einwirken lässt. Das neue Derivat der p-Nitrobenzoylessigsäure entspricht der Formel
EMI0001.0008
und stellt ein hellgelbes kristallines Pulver dar. Das neue Produkt vereinigt sich mit 5-Nitro-2-diazoanisol in Substanz oder auf einer geeigneten Grundlage, wie z.
B. pflanz liche Faser, zu einem echten gelben Farbstoff. <I>Beispiel:</I> Man erwärmt ein Gemisch von 23,7 Teilen p-Nitrobenzoylessigester und 200 Teilen Xylol in einem mit absteigendem Rührer versehenen Rührgefäss auf 130-140 . Bei dieser Tem peratur trägt man 21,2 Teile p-Aminobenzoyl- anilin ein. Es setzt Alkoholabspaltung ein, der abdestilliert wird.
Man kondensiert etwa 5 Stunden, treibt dann das Xylol mit Wasser dampf ab und löst den Rückstand in ver dünnter Natriiimhydroxydlösung, filtriert und säuert aus. Zur Reinigung kann das Produkt aus Eisessig umkristallisiert werden.
Process for the preparation of a derivative of p-nitrobenzoyl acetic acid. It has been found that a new derivative of p-nitrobenzoyl acetic acid is obtained if 1 mole of p-aminobenzoylaniline is allowed to act on 1 mole of p-nitroberizoyl acetic ester. The new derivative of p-nitrobenzoyl acetic acid corresponds to the formula
EMI0001.0008
and represents a light yellow crystalline powder. The new product combines with 5-nitro-2-diazoanisole in substance or on a suitable basis, such as.
B. vegetable fiber, to a real yellow dye. <I> Example: </I> A mixture of 23.7 parts of p-nitrobenzoyl acetic ester and 200 parts of xylene is heated to 130-140 in a stirred vessel equipped with a descending stirrer. At this temperature, 21.2 parts of p-aminobenzoylaniline are entered. Alcohol is split off, which is distilled off.
The condensation is carried out for about 5 hours, then the xylene is driven off with steam and the residue is dissolved in dilute sodium hydroxide solution, filtered and acidified. For cleaning, the product can be recrystallized from glacial acetic acid.
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH173735T | 1934-01-23 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH173735A true CH173735A (en) | 1934-12-15 |
Family
ID=4424935
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH173735D CH173735A (en) | 1934-01-23 | 1934-01-23 | Process for the preparation of a derivative of p-nitrobenzoyl acetic acid. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH173735A (en) |
-
1934
- 1934-01-23 CH CH173735D patent/CH173735A/en unknown
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