CH203629A - Process for the production of a condensation product. - Google Patents
Process for the production of a condensation product.Info
- Publication number
- CH203629A CH203629A CH203629DA CH203629A CH 203629 A CH203629 A CH 203629A CH 203629D A CH203629D A CH 203629DA CH 203629 A CH203629 A CH 203629A
- Authority
- CH
- Switzerland
- Prior art keywords
- production
- condensation product
- orange
- nitro
- cyanobenzene
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B51/00—Nitro or nitroso dyes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
<B>Zusatzpatent</B> zum Hauptpatent Nr. 200069: Verfahren zur Herstellung eines Kondensationsproduktes. Vorliegendes Patent bezieht sich auf ein Verfahren zur Herstellung eines Kondensa tionsproduktes, dadurch gekennzeichnet, dass man 1-Chlor-2-nitro-4-cyanbenzol mit p-Amino- phenol kondensiert.
Das so erhaltene 2-Nitro-4-cyan-4'-ogy- diphenylamin kristallisiert aus Methanol in orangegelben Kristallen vom Smp. <B>175</B> und färbt und druckt Acetatseide in orangegelben Tönen von hervorragender Lichtechtheit.
<I>Beispiel:</I> 18,5 Teile 1-Chlor-2-nitro-4-cyanbenzol werden mit etwa 120 Teilen Alkohol und 25 Teilen p-Aminophenol mehrere Stunden unter Rückflusskühlung zum Sieden erhitzt. Beim Erkalten scheidet sich das gebildete Kondensationsprodukt in orangegelben Kri stallen aus.
<B> Additional patent </B> to main patent no. 200069: Process for the production of a condensation product. The present patent relates to a process for the production of a condensation product, characterized in that 1-chloro-2-nitro-4-cyanobenzene is condensed with p-aminophenol.
The 2-nitro-4-cyano-4'-ogydiphenylamine obtained in this way crystallizes from methanol in orange-yellow crystals with a melting point of 175 and dyes and prints acetate silk in orange-yellow shades of excellent lightfastness.
<I> Example: </I> 18.5 parts of 1-chloro-2-nitro-4-cyanobenzene are refluxed with about 120 parts of alcohol and 25 parts of p-aminophenol for several hours. On cooling, the condensation product formed separates out in orange-yellow crystals.
Claims (1)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE203629X | 1936-08-28 | ||
| CH200069T | 1937-08-11 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH203629A true CH203629A (en) | 1939-03-15 |
Family
ID=25723438
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH203629D CH203629A (en) | 1936-08-28 | 1937-08-11 | Process for the production of a condensation product. |
Country Status (1)
| Country | Link |
|---|---|
| CH (1) | CH203629A (en) |
-
1937
- 1937-08-11 CH CH203629D patent/CH203629A/en unknown
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